Medical Device Manufacturer · US , Crofton , MD

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

17 submissions · 17 cleared · Since 1987

Total

Cleared

Denied

Marquette Medical, Inc. has 17 FDA 510(k) cleared general hospital devices. Based in Crofton, US.

Historical record: 17 cleared submissions from 1987 to 2003.

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

Marquette Medical, 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 - Marquette Medical, Inc.

17 devices

1-12 of 17

Cleared Sep 08, 2003

MARQUETTE HUBER TRAP SAFETY INFUSION SET

K021471 · FPA

General Hospital · 488d

Cleared Jan 11, 1996

INFANT FEEDING TUBE

K953008 · FPD

Gastroenterology & Urology · 197d

Cleared Sep 15, 1995

PLASTIC BLUNT CANNULA

K952976 · FPA

General Hospital · 80d

Cleared Oct 13, 1992

SUBCUTANEOUS INFUSION SET

K920537 · FPA

General Hospital · 251d

Cleared Jun 04, 1991

4 LOW VOLUME IV EXTENSION SET WITH SLIDE CLAMP

K905218 · FPA

General Hospital · 196d

Cleared Jun 04, 1991

4' LOW VOLUME IV EXTENSION SET

K905219 · FPA

General Hospital · 196d

Cleared May 31, 1991

IV EXTENSION SETS WITH .22 MICRON FILTER

K905374 · FPA

General Hospital · 183d

Cleared Oct 04, 1990

LOW VOLUME BIFURCATED IV EXTENSION SET

K901088 · FPA

General Hospital · 211d

Cleared Oct 04, 1990

LOW VOLUME TRIFURCATED IV EXTENSION SET

K901089 · FPA

General Hospital · 211d

Cleared Feb 28, 1990

IV BIFURCATED EXTENSION SET

K900426 · FPA

General Hospital · 29d

Cleared Feb 28, 1990

IV TRIFURCATED EXTENSION SET

K900427 · FPA

General Hospital · 29d

Cleared Oct 17, 1988

STRAIGHT AND RIGHT ANGLE NON-CORING NEEDLES

K884211 · FMI

General Hospital · 11d

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

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

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