Medical Device Manufacturer · US , Southbridge , MA

Henke Sass Wolf of America, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1994

Total

Cleared

Denied

Henke Sass Wolf of America, Inc. has 9 FDA 510(k) cleared medical devices. Based in Southbridge, US.

Historical record: 9 cleared submissions from 1994 to 2008.

Browse the FDA 510(k) cleared devices submitted by Henke Sass Wolf of America, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Henke Sass Wolf of America, Inc.

9 devices

1-9 of 9

Cleared Mar 18, 2008

HENKE SASS WOLF OF AMERICA ARTHROSCOPE

K080560 · HRX

Orthopedic · 19d

Cleared Mar 24, 2005

HENKE SASS WOLF OF AMERICA BARIATRIC LAPAROSCOPE

K050163 · GCJ

General & Plastic Surgery · 58d

Cleared Apr 01, 2003

HENKE SASS WOLF OF AMERICA NASOPHARYNGOSCOPE

K030572 · EOB

Ear, Nose, Throat · 36d

Cleared Feb 01, 2002

HENKE SASS WOLF SAPHENOUS VEIN LAPAROSCOPE

K013611 · GCJ

General & Plastic Surgery · 88d

Cleared Oct 13, 1999

CONTINUOUS FLOW HYSTERO-RESECTOSCOPE, KNIFE ELECTRODE, SPIKE ELECTRODE,...

K991563 · HIH

Obstetrics & Gynecology · 161d

Cleared Oct 30, 1998

FINE-JECT

K983067 · FMI

General Hospital · 58d

Cleared Aug 13, 1998

SINUSCOPE AND ACCESSORIES

K981751 · EOB

Ear, Nose, Throat · 87d

General & Plastic Surgery · 48d

Henke Sass Wolf of America, Inc. - FDA 510(k) Cleared Devices

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