Medical Device Manufacturer · US , Walker , MI

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

16 submissions · 16 cleared · Since 1983

Total

Cleared

Denied

Taut, Inc. has 16 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 16 cleared submissions from 1983 to 2002. Primary specialty: General & Plastic Surgery.

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

Taut, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

16 devices

1-12 of 16

Cleared Dec 13, 2002

ADAPT BALLOON OPEN ACCESS PORT, MODEL 41244

K023261 · GCJ

General & Plastic Surgery · 74d

Cleared Aug 08, 2002

ADAPT OPEN ACCESS PORT, MODEL 41233

K021731 · GCJ

General & Plastic Surgery · 76d

Cleared Jun 22, 2001

TAUT BALLOON CATHETER, MODEL 50640

K011018 · GCA

Gastroenterology & Urology · 79d

Cleared Feb 22, 2001

TAUT-INSUFFLATION NEEDLE

K003703 · HIF

Obstetrics & Gynecology · 83d

Cleared Feb 22, 2001

ADAPT LAPAROSCOPIC PORT & ADAPT REDUCER CAP

K010007 · GCJ

General & Plastic Surgery · 51d

Cleared Oct 05, 1999

MINI-PORT

K992904 · GBW

General & Plastic Surgery · 36d

Cleared Oct 05, 1999

INTRADUCER

K992907 · GBW

General & Plastic Surgery · 36d

Cleared Dec 01, 1997

INTRADUCER PORT SC CATALOG#31275,31035,30915, AND 31450

K972112 · GBW

General & Plastic Surgery · 179d

Cleared Jul 18, 1996

TUAT SPLATTER CONTROL SHIELD SCS-300

K962003 · KKX

General Hospital · 57d

Cleared Mar 20, 1996

INTRADUCER PERITONEAL CATHETER 6FRX3, 9FRX3 1/2, 10FRX4, 12FRX8

K960883 · GCJ

General & Plastic Surgery · 15d

Cleared Feb 28, 1995

SPLATTER CONTROL SHIELD

K945486 · KKX

General Hospital · 112d

Cleared Apr 06, 1993

OPERATIVE CHOLANGIOGRAM CATHETER

K924981 · GBZ

General & Plastic Surgery · 187d

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

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

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