Diasonics, Inc.
Diasonics, Inc. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1997.
Top product codes for Diasonics, Inc.
Recent clearances by Diasonics, Inc.
- K962662 — VINGMED SOUND COLOR FLOW MAPPING SYSTEM
- K924079 — CFM-800 COLOR FLOW MAPPING SYSTEM
- K911435 — CPA/3.5 MHZ PROBE
- K905200 — SACA, 3.5 MHZ PROBE
- K903562 — CW DOPPLER 2.25 MHZ PROBE
- K903984 — CW DOPPLER/4.5 MHZ
- K896637 — ACCESS(TM), SOFTWARE RELEASE 4.11P
- K893518 — MT/S SOFTWARE RELEASE 5.0.
- K894290 — ACCESS TM
- K893881 — ACCESS TM
- K891452 — SPECTRA ULTRASOUND SYSTEM W/COLOR FLOW MODULE
- K891541 — MAGNETIC RESONANCE DEVICE ACCESSORY SOFTWARE 4.0.
- K884816 — ACCESS(TM) MAGNETIC RESONANCE DEVICE ACCESSORY
- K884607 — MT/S (SOFTWARE RELEASE 3.1)
- K884606 — MT/S (SPINE TRANSMIT COIL)
- K884743 — TEMPOROMANDIBULAR JOINT COIL (TMJ)
- K884603 — SHOULDER TRANSMIT AND RECEIVE COILS
- K884604 — MT/S CARLSON SPINE COIL, PART # 100-50082500-01
- K882478 — 100-01778-52 ULTRASOUND SYSTEM
- K883516 — DIASONICS MT/P IMAGING SYSTEM
- K880714 — DIASONICS QT ENDORECTAL 7.5 MHZ PROBE
- K870967 — ADMS TRANSRECTAL 7.5 MHZ PROBE
- K864908 — DIASONICS TRANSVAGINAL, TV 7.5 MHZ PROBE
- K864758 — DIASONICS SPA 5.O 27MM PROBE
- K864812 — DIASONICS SPA 3.5 MHZ, 30MM PROBE
- K863780 — ADA-1000 (ADVANCED DIGITAL ARRAY)
- K860361 — DIASONICS 3.5 GWA 30MM PROBE
- K853432 — 5.0 IOP & 7.5 IOP PROBES
- K851972 — DIASONICS ADA400 ADVANCED DIGITAL ARRAY
- K851446 — UNIVERSAL SERVICE MODULE
- K851860 — DIASONICS DRF-200 ULTRASOUND IMAGING SYSTEM
- K851973 — DIASONICS, BERGER STEREOTACTIC NEOROBIOPSY
- K833667 — DIASONICS DLA-100
- K831317 — BIOPSY ATTACHMENT
- K827573 — DIASONICS CARDIO/IMAGING ECHOSCOPE
- K820820 — CARDIO REVUE CENTER
- K820033 — CARDIOVUE ACCESSORY CART
- K813217 — DIGITAL FLUROGRAPHIC IMAGING SYSTEM
- K812515 — CARDIAC REVIEW STATION
- K811556 — DC-1 CARDIAC IMAGING MODULE
- K802979 — DIASONICS SMALL PARTS SCANNER
- K781642 — RA-I
Data sourced from openFDA. This site is unofficial and independent of the FDA.