Medasonics, Inc.
Medasonics, Inc. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1999.
Top product codes for Medasonics, Inc.
Recent clearances by Medasonics, Inc.
- K991441 — CADENCE DOPPLER ULTRASOUND SYSTEM
- K962796 — NEUROGUARD TRANSCRANIAL DOPPLER ULTRASOUND SYSTEM
- K961116 — FIRST BEAT/CARDIO BEAT/CALC
- K914862 — CEREBROVASCULAR DIAGNOSTIC SYSTEM; CDS
- K911453 — OBTRASOUND STETHOSCOPE FETAL CALC
- K882018 — MEDACORD PVL, PERSONAL VASCULAR LABORATORY
- K872292 — TRANSPECT TRANSCRANIAL DOPPLER
- K854734 — MODEL 5320 TED SEQUENTIAL COMP. DE. COMP. LIMB SLE
- K833588 — VASCULAR LABORATORY TREADMILL VT1
- K837481 — BF24 DOPPLER MODEL P872 AND P874
- K831393 — VASCULAB BLOOD PRESSURE CUFF
- K820898 — VASCULAB SPECTRUM ANALYZER #SP25
- K812608 — VASCULAB #R12B
- K812609 — VASCULAB #VSC21
- K801549 — MODEL R11 SINGLE CHANNEL CHART RECORDER
- K800768 — VASCULAB BI-DIRECTIONAL DOPPLER, #D10
- K800767 — MOD. MCI 17 MANUAL CUFF INFLATOR
- K782132 — PLETHYSMOGRAPH, STRAIN GAUGE
- K781358 — SEQUENTIAL CUFF INFLATION DEVICE
Data sourced from openFDA. This site is unofficial and independent of the FDA.