Sonicaid, Inc.
Sonicaid, Inc. holds FDA 510(k) medical device clearances, first cleared 1977, most recent 1988.
Top product codes for Sonicaid, Inc.
Recent clearances by Sonicaid, Inc.
- K873673 — BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONAL
- K872074 — 5 MHZ TRANSDUCER
- K863803 — VASOPULSE(TM)/MODEL 5000
- K862720 — VASOFLO-3 & EXTRAVASCULAR BLOOD FLOW PROBES
- K861237 — VASOVIEW DUPLEX IMAGING SYSTEM
- K851102 — VASOSCREEN IMPEDANCE PLETHYSMOGRAPH
- K833902 — VASOSCAN
- K832374 — PHOTOFLO DUAL-MODE PHOTOPLETHYSMOGRAPH
- K833488 — SONICOMP
- K833227 — SONICAID MODEL D206E AIR EMBOLI-DETECT
- K831371 — MODEL FM5
- K812256 — MODEL AP 180 MINI-MONITOR
- K803246 — ULTRASONIC STETHOSCOPE
- K800858 — FETAL HEART DETECTOR #'S D102 & D102R
- K800859 — FETAL HEART DETECTOR #D206
- K790678 — INTRAUTERINE CATHETER TIP
- K780487 — FETAL MONITORING SYSTEM
- K771379 — FETAL MONITORING SYS. MODEL FM3R
Data sourced from openFDA. This site is unofficial and independent of the FDA.