Medical Device Manufacturer · US , Pittsburgh , PA

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

8 submissions · 8 cleared · Since 1986

8

Total

8

Cleared

0

Denied

Micor, Inc. has 8 FDA 510(k) cleared medical devices. Based in Pittsburgh, US.

Historical record: 8 cleared submissions from 1986 to 2003.

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

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

8 devices

1-8 of 8

Cleared Aug 13, 2003

CONDUCTION CATHETER

General Hospital · 84d

Cleared Jul 17, 2001

WUNDCATH CONDUCTION CATHETER

General Hospital · 207d

Cleared Sep 20, 2000

MICOR CONDUCTION CATHETER

Anesthesiology · 107d

Cleared Aug 11, 2000

MICOR ANESTHESIA CONDUCTION KIT

Anesthesiology · 46d

Cleared Oct 28, 1999

SPRING-WOUND EPIDURAL CATHETER

Anesthesiology · 148d

Cleared Apr 29, 1986

PERCUTANEOUS CATHETERS

Cardiovascular · 42d

Cleared Mar 31, 1986

PERCUTANEOUS CATHETERS

Cardiovascular · 61d

Cleared Jan 16, 1986

ANGIOGRAPHY CATHETERS

Cardiovascular · 108d