Medical Device Manufacturer · US , Newton , NC

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

6 submissions · 6 cleared · Since 1992

Recent clearances: SAFETY NEEDLE, S-MONOVETTE EDTA K2-GEL, SAFETY-MULTIFLY

View 6 510(k) Devices ↓

6

Total

6

Cleared

0

Denied

Sarstedt, Inc. has 6 FDA 510(k) cleared medical devices. Based in Newton, US.

Historical record: 6 cleared submissions from 1992 to 2005.

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

Sarstedt, Inc. is one of 24517 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

6 devices

1-6 of 6

Cleared Jul 25, 2005

Chemistry · 94d

Cleared Sep 12, 2003

S-MONOVETTE EDTA K2-GEL

Chemistry · 135d

Cleared Sep 12, 2003

SAFETY-MULTIFLY

General Hospital · 60d

Cleared Apr 14, 2003

URINE MONOVETTE BORIC ACID

Microbiology · 112d

Cleared Mar 30, 2001

SARSTEDT NEEDLE PROTECTOR

General Hospital · 150d

Cleared Jan 31, 1992

Hematology · 170d