Medical Devices, Inc.
Medical Devices, Inc. holds FDA 510(k) medical device clearances, first cleared 1977, most recent 2001.
Top product codes for Medical Devices, Inc.
Recent clearances by Medical Devices, Inc.
- K002280 — PAD PRO PEDIATRIC ELECTRODE, MODEL PAD PRO 2602
- K930084 — MICRO-ARTHROSCOPE
- K940012 — SMARTBRACE ELECTRODE
- K943126 — ELECTROFLEX
- K935132 — HOME MICROCURRENT HMC
- K934619 — FLEXMATE
- K924897 — XENON ENDOSCOPIC ILLUMINATOR, MODEL XEI-300
- K930053 — VIDEO CAMERA W/ ELECTRONIC SHUTTER MODEL VCE-10
- K923914 — IF-II (TM), MODEL 7200
- K920071 — MEDITRON AUTOMATIC ELECTRONIC INSUFF. MODEL AEI-15
- K915694 — MEDITRON ELECTRONIC LAPAROSCOPIC INSUFFLATOR
- K915408 — BIPOLAR ENDOSTASIS PROBE, BEST (TM)
- K912182 — MEDITRON COMBINATION GENERATOR CG-2000
- K912348 — SX90 (TM),MODEL 4800S
- K905133 — STYLET TRACHAEL TUBE
- K903161 — MC II (TM), MODEL 7200S
- K901302 — BIPOLARD POLYPECTOMY SYSTEM (TM)
- K895473 — DSX(TM), DIGITAL SX, QUANTUM DSX, MODEL 4700S
- K883462 — IF-II (TM), MODEL 9800
- K890705 — MEDIMOD(TM), MODEL 8900
- K882888 — MULTIDAY, MODELS 8300 AND 8310
- K882886 — PROGEL (TM) DUAL ELECTRODE PAD, MODEL 8535
- K882887 — PROGEL(TM), MODELS 8630 AND 8635
- K882820 — MEDIPAC II EC (TM), MODEL 7900
- K881082 — GV 11 (TM), MODEL 9700
- K872753 — MYOSTIM(TM), MODEL 6600
- K872657 — ULTRAPAC II SX PLUS (TM)
- K864968 — BACPAC (TM), MODEL 6500
- K864625 — MYOPAC (TM), MODEL 9600
- K862337 — ULTRAPAC II SD (TM)
- K862028 — ULTRAHESIVE II POSTOP ELECTRODE
- K861011 — SILENT PARTNER MODEL 10-2001
- K861012 — SILENT PARTNER MODEL 10-1001
- K854316 — FASTENS(TM)
- K854761 — MINIPAC PERSONAL TOUCH (TM)
- K854317 — MINIPAC (TM)
- K851175 — TRANSCUTANEOUS ELECTRICAL NERVE STIMULA-ELECTORDE
- K831413 — SPEC IISX
- K821979 — STERILE FOLEY CATHETERIZATION KITS
- K821978 — STERILE URETHRAL CATHETERIZATION SET
- K810593 — NEUROPAC ULTRA I
- K803259 — CLOSED SYSTEM URETHRAL CATHETERIZ. SET
- K792312 — HEART RATE MONITOR MD-1
- K792082 — GAVAGE FEEDING SET
- K781829 — NEUROPAC ULTRA II
- K780831 — URINARY CATHETERIZATION SYSTEM W/O FOLEY
- K780134 — URINARY DRAINAGE MONITORING SYSTEM
- K771779 — CATHETERIZATION SYS. URINARY DRAINAGE
- K770320 — URINARY DRAINAGE SET, CLOSED, STERILE
Data sourced from openFDA. This site is unofficial and independent of the FDA.