Philips Medical Systems (Cleveland), Inc.
Philips Medical Systems (Cleveland), Inc. holds FDA 510(k) medical device clearances, first cleared 1977, most recent 2017, with 315 FDA device recalls on record.
Clearances by Philips Medical Systems (Cleveland), Inc. — page 2
101–190 of 190- K944469 — GENERAL PURPOSE FLEX COIL
- K943415 — MERIT (O.1T MR SYSTEM)
- K944973 — NRF SYSTEM
- K944987 — URO - ELITE TABLE ACCESSORIES
- K943447 — V-MAX OPTIONS
- K943926 — RAPIDO 2000 AUTOMATIC RADIOGRAPHIC TABLE
- K941996 — EDGE
- K941408 — MERIT
- K940721 — CLINIX VP 4 TABLE
- K933356 — MERIT
- K931544 — 1.5T EDGE AND 1.0T VISTA SYSTEMS
- K933835 — 0.5T ASSET SYSTEM
- K932693 — EDGE SYSTEM
- K931998 — LCR GENERATOR
- K925845 — VISTA HP/HPQ SYSTEM
- K923851 — ACQSIM SIMULATOR/LOCALIZER
- K923615 — VISTA HPQ SYSTEM
- K920714 — VISTA HPQ SYSTEM
- K921881 — VISTA HPQ SYSTEM
- K921609 — VISTA HP/HPQ SYSTEM
- K920199 — HEAD COIL GEOMETRIC DISTOR SPEC FOR VISTA HPQ SYST
- K914376 — DXS DIGITAL X-RAY SUBTRACTION
- K913534 — VISTA HPQ SYSTEM
- K910715 — VISTA HPQ SYSTEM
- K905259 — VISTA HPQ SYSTEM
- K905070 — VISTAR
- K904050 — MODEL DH-1000 SINGLE DETEC./DUAL DETEC NUCL CAMERA
- K903048 — VISTA MR 2055 HP SYSTEM
- K900064 — VISTA HPQ SYSTEM, VISTA MR 2055 HP SYSTEM
- K896508 — VISTA MR 2055 HP SYSTEM
- K895151 — VISTA MR 2055 HP SYSTEM
- K893675 — VISTA MR 2055 HP SYSTEM AND 2055 UPGRADES
- K893739 — VISTA MR 2055 HP SYSTEM AND 2055 UPGRADES
- K893619 — VISTA MR 2055 HP SYSTEM
- K885047 — VISTA MR 2055 HP SYSTEM
- K883580 — UNIVERSAL ABC CONTROLER
- K883994 — VISTA MR 2055 HP SYSTEM
- K883482 — VISTA MR 2055 HP SYSTEM
- K883519 — FAST AND CE-FAST MRI SEQUENCES (FOR NMR 1000)
- K882378 — P-7 COMPUTED TOMOGRAPHY SYSTEM
- K883520 — 0.5 T COMPACT MAGNET FOR ITS VISTA MR 2055 HP SYST
- K883378 — VISTA MR 2055 HP SYSTEM
- K883521 — C/R GATING FOR ITS VISTA MR 2055/2055 UP & HP SYS
- K880878 — CX250 MOBILE GAMMA CAMERA & DCS CONSOLE
- K880352 — MTX GENERATOR
- K881185 — ANNULAR ARRAY PROBES FOR ARTIS 3200 DIAG. ULTRA.
- K875251 — ARTIS 3200 DIAGNOSTIC ULTRASOUND DEVICE
- K862593 — DAS 211
- K862452 — MX MOBILE X-RAY SYSTEM
- K853565 — ARTIS ULTRASOUND IMAGING SYSTEM
- K860129 — ISO-MAMMO
- K854328 — MEDEX X-RAY TABLE
- K855213 — PET-SCOPE II IMAGE INTENSIFIER
- K850823 — SRX 200 DIAGNOSTIC X-RAY, HIGH VOLTAGE GENERATOR
- K850125 — MULTI-SIZE CASSETTE HOLDER
- K834212 — N-CHANNEL
- K843192 — APR MOBILE
- K842055 — PICKER ARTIS ULTRASOUND IMAGING SYS
- K834211 — LEAP FROG
- K813002 — MAVIS C
- K813279 — ELECTROCARDIOGRAPH CM3000
- K811629 — DYNA- MO
- K811934 — DSS 500
- K811967 — CP-625 SEE-THRU FILM CHANGER
- K811969 — DUAL PEDESTAL TABLE
- K811970 — AP X-RAY TUBE ANGULATION DEVICE
- K811198 — ECCO GENERATOR
- K811295 — DIGITAL NOISE REDUCER
- K810973 — SYSTEM 400
- K810797 — LOW DOSE SERVOCHEST
- K810274 — CLINIX-R TOMOGRAPHIC DEVICE
- K803049 — DIGITAL RADIOGRAPHY CHEST DEVICE
- K810183 — PRO-TOP-ANGIO SHIFT TABLE TOP EXTENSION
- K810194 — WALL CASSETTE HOLDER - TRAC44
- K810118 — LS1000 ELECTRONIC FOCUS
- K802996 — VECTOR-100 X-RAY GENERATOR
- K802578 — PACE-4-AUTOMATIC RIA GAMMA-COUTER
- K801407 — SYNERVIEW MODEL 6545
- K801408 — CINESCOPE III
- K800805 — LINEAR ARRAY SCANNER
- K800639 — ORBITOR
- K800554 — MULTI-FORMAT SFD MODEL 1720
- K790489 — MICROVIEW
- K781709 — SCANNER, LINEAR
- K781425 — CAP-MOBILE
- K781473 — BUCKY WALL STAND
- K780313 — HITACHI TECH-MOBLE DHC-121
- K780319 — ORBITOME-UG
- K772123 — TOMOGRAPHIC SYSTEM, COMPUTERIZED
- K770855 — SYNERVIEW MODEL 6478
Data sourced from openFDA. This site is unofficial and independent of the FDA.