Biosound, Inc.
Biosound, Inc. holds FDA 510(k) medical device clearances, first cleared 1983, most recent 1997.
Top product codes for Biosound, Inc.
Recent clearances by Biosound, Inc.
- K971700 — BIOPSY ACCESSORY FOR ULTRASOUND TRANSDUCER
- K963936 — ACCESSPOINT, MED E-MAIL, DICOM READER
- K963262 — ARTOSCAN M
- K963662 — GALILEO EVOKED POTENTIALRE
- K953716 — INTRACAVITY TRANSDUCERS
- K953530 — DIAGNOSTIC ULTRASOUND TRANDUCERS P10A, P12A, PT10A, PA11-A
- K953759 — DIAGNOSTIC ULTRASOUND TRANSDUCER
- K953819 — DIAGNOSTIC ULTRASOUND TRANDUCER
- K955458 — ULTRASOUND PROBE BIOPSY ACCESSORIES
- K953579 — TEE PROBE
- K953430 — ULTRASOUND PROBE BIOPSY ACCESSORIES
- K941935 — LP-12 LAPAROSCOPIC PROBE
- K944287 — 7050 ULTRASOUND IMAGING SYSTEM
- K944485 — 4000 AU ULTRASOUND IMAGING SYSTEM
- K934050 — TOPOGRAPHIC BRAIN MAPPING OPTION
- K931022 — ARTOSCAN
- K922703 — THE ACTA FORMULA
- K923894 — YHE GALILEO PLEIADE ELECTROENCEPHALOGRAPH
- K922488 — PHASIS ELECTROMYOGRAPH
- K923860 — THE GALILEO LINE -- PLANET 100, 200 & 300 & STAR
- K923950 — THE GALILEO VEGA-24 ELECTROENCEPHALOGRAPH
- K922291 — PERSONAL 120/210 LAPTOP STRESS OPTION
- K915860 — LINEAR PERIPHERALVASCULAR ULTRSOUND PROBE
- K913209 — ACCESSORY TO GENESIS III (GCFM)
- K914006 — BIPLANE TRANSRECTAL PROBE
- K920364 — ELECTROCARDIOGRAPH STRESS TEST FIRMWARE ACTAVIS
- K912088 — BIOPSY ACCESSORIES FOR ULTRASOUND PROBES
- K895645 — BIOSOUND PHASE 2 DIAGNOSTIC ULTRASOUND SYSTEM
- K894370 — GENESIS III, (MOD. 7003/7004)
- K894163 — PHASE 2 TRANSCRANIAL PROBE
- K883238 — GENESIS II TRANSCRANIAL PROBE
- K881723 — GENESIS II 7.5MHZ ULTRASOUND TRANSDUCER
- K871442 — BIOSOUND MMI ULTRASOUND
- K873032 — GENESIS II, 2.5/5.0 MHZ S.E/5.0MHZ/3.5 16/19 MM AN
- K870899 — EZU-PC 2A/5.0 & 3A/3.5MHZ, EUP-CD 121/5.0 CONVEX
- K871697 — GENESIS II
- K862859 — EUB 151 ULTRASOUND SYSTEM/EUB 150 ULTRASOUND
- K862841 — HIGH VELOCITY CW DOPPLER SYSTEM
- K837063 — BIOSOUND SURGISCAN, ULTRASOUND IMAGING SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.