Medical Device Manufacturer · US , Indianapolis , IN

Biosound, Inc. - FDA 510(k) Cleared Devices

39 submissions · 39 cleared · Since 1983

Total

Cleared

Denied

Biosound, Inc. has 39 FDA 510(k) cleared medical devices. Based in Indianapolis, US.

Historical record: 39 cleared submissions from 1983 to 1997. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Biosound, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Biosound, Inc.

39 devices

1-12 of 39

Cleared Jul 09, 1997

BIOPSY ACCESSORY FOR ULTRASOUND TRANSDUCER

K971700 · ITX

Radiology · 62d

Cleared Mar 31, 1997

ACCESSPOINT, MED E-MAIL, DICOM READER

GALILEO EVOKED POTENTIALRE

K963662 · GWF

Neurology · 166d

Cleared Apr 17, 1996

INTRACAVITY TRANSDUCERS

K953716 · ITX

Radiology · 252d

Cleared Apr 08, 1996

DIAGNOSTIC ULTRASOUND TRANDUCERS P10A, P12A, PT10A, PA11-A

K953530 · IYO

Radiology · 256d

Cleared Mar 01, 1996

DIAGNOSTIC ULTRASOUND TRANSDUCER

K953759 · ITX

Radiology · 203d

Cleared Mar 01, 1996

DIAGNOSTIC ULTRASOUND TRANDUCER

K953819 · ITX

Radiology · 199d

Cleared Feb 12, 1996

ULTRASOUND PROBE BIOPSY ACCESSORIES

ULTRASOUND PROBE BIOPSY ACCESSORIES

K953430 · ITX

Radiology · 95d

Cleared Sep 18, 1995

LP-12 LAPAROSCOPIC PROBE

K941935 · ITX

Radiology · 516d

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Biosound, Inc. - FDA 510(k) Cleared Devices

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