Medical Device Manufacturer · US , Waterford , WI

Continental Medical Laboratories, Inc. - FDA 510(k) Cleared Devices

8 submissions · 6 cleared · Since 1991

8

Total

6

Cleared

0

Denied

Continental Medical Laboratories, Inc. has 6 FDA 510(k) cleared medical devices. Based in Waterford, US.

Historical record: 6 cleared submissions from 1991 to 1997. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Continental Medical Laboratories, Inc.

8 devices

1-8 of 8

Cleared Feb 14, 1997

PROD. NO. 01-132 - SUTURE REMOVAL KIT

General & Plastic Surgery · 74d

Cleared Oct 21, 1996

STAPLE REMOVAL KIT

General & Plastic Surgery · 63d

Cleared Oct 17, 1996

PROD. NO. 02-031 - LACERATION TRAY

General & Plastic Surgery · 48d

Cleared Oct 11, 1996

TRACHEOSTOMY CLEANING TRAY W/SUCTION CATHETER

Anesthesiology · 136d

Cleared Sep 23, 1996

PROD NO. 01-1694 - 4X4 FOAM DRESSING

General & Plastic Surgery · 346d

Cleared Jun 21, 1996

URETHRAL CATHETERIZATION TRAY/UNIVERSAL URETHRAL CATH TRAY

Gastroenterology & Urology · 24d

Cleared Jun 14, 1995

WOUND CARE MANAGEMENT KITS

General Hospital · 27d

Cleared Mar 27, 1991

G-TUBE DRESSING CHANGE TRAY

General & Plastic Surgery · 133d