Medical Device Manufacturer · US , Santa Ana , CA

Kendall Mcgaw Laboratories, Inc. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1986

13

Total

13

Cleared

0

Denied

Kendall Mcgaw Laboratories, Inc. has 13 FDA 510(k) cleared general hospital devices. Based in Santa Ana, US.

Historical record: 13 cleared submissions from 1986 to 1991.

Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.

Kendall Mcgaw Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Kendall Mcgaw Laboratories, Inc.

13 devices

1-13 of 13

Cleared Mar 01, 1991

MICRORATE INTELLIGENT PUMP

General Hospital · 80d

Cleared Mar 01, 1991

MICRORATE PLUS INTELLIGENT PUMP

General Hospital · 80d

Cleared Nov 19, 1990

General Hospital · 21d

Cleared Oct 17, 1990

VOLUMETRIC INFUSION PUMP

General Hospital · 14d

Cleared Oct 03, 1990

PROTECTED NEEDLE WITH OR WITHOUT IV SET

General Hospital · 44d

Cleared Aug 21, 1990

General Hospital · 167d

Cleared Jul 11, 1990

ADD-A-VIAL II BINARY CONNECTOR

General Hospital · 138d

Cleared Dec 08, 1989

1.2 MICRON FILTER WITH IV SET

General Hospital · 38d

Cleared Sep 27, 1989

SECONDARY IV SET WITH PROTECTED NEEDLE

General Hospital · 43d

Cleared Aug 24, 1988

522 INTELLIGENT PUMP

General Hospital · 93d

Cleared Jan 06, 1988

SET, ADMINISTRATION INTRAVASCULAR

General Hospital · 65d

Cleared Oct 03, 1986

MCGAW NUTRA-FEED EFS ENTERAL FEEDING BAG

Gastroenterology & Urology · 123d

Cleared Aug 14, 1986

MCGAW NUTRA-FEED EFS ENTERAL FEEDING TUBE

Gastroenterology & Urology · 73d