Medical Device Manufacturer · US , Mchenry , IL

Burron Medical Products, Inc. - FDA 510(k) Cleared Devices

41 submissions · 40 cleared · Since 1979

Total

Cleared

Denied

Burron Medical Products, Inc. has 40 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 40 cleared submissions from 1979 to 1987. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Burron Medical Products, Inc.

41 devices

1-12 of 41

Cleared May 01, 1987

CAVAFIX(R) CENTRAL VENOUS CATHETER KIT W/SUTURE

K870403 · FOZ

General Hospital · 88d

Cleared Nov 13, 1986

INTESTOPLANT

K862412 · LLD

General Hospital · 141d

Cleared Jul 01, 1986

CAVAFIX, CENTRAL VENOUS CATHETER KIT

K861479 · FOZ

General Hospital · 70d

Cleared Feb 28, 1986

STIMUPLEX, NERVE STIMULATOR

General Hospital · 283d

Cleared Jul 09, 1984

JEJUNOSTOMY SET FOR TUBE FEEDING

K841428 · KNT

Gastroenterology & Urology · 94d

Cleared May 01, 1984

LONG TERM CENTRAL VENOUS ACCESS CATH

K834299 · LJS

General Hospital · 145d

Cleared May 01, 1984

DUAL-LUMEN LONG TERM CENTRAL VENOUS CAT

K834383 · LJS

General Hospital · 139d

Cleared Apr 30, 1984

MULTI-LUMEN CENTRAL VENOUS CATH. KIT

K834473 · LJS

General Hospital · 132d

Cleared Feb 24, 1984

CONTINUOUS EPIDURAL ANESTHES. TRAY

K840179 · CAZ

Anesthesiology · 38d

Cleared Feb 23, 1984

BRACHIAL PLEXUS ANESTHESIA TRAY

General Hospital · 29d

Looking for a specific device from Burron Medical Products, Inc.? Search by device name or K-number.

Search all Burron Medical... devices

Burron Medical Products, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Burron Medical Products, Inc.

Filters