Marquette Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Marquette Medical, Inc. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
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.
FDA 510(k) Regulatory Record - Marquette Medical, Inc.
17 devices
Cleared
Sep 08, 2003
MARQUETTE HUBER TRAP SAFETY INFUSION SET
General Hospital
488d
Cleared
Jan 11, 1996
INFANT FEEDING TUBE
Gastroenterology & Urology
197d
Cleared
Sep 15, 1995
PLASTIC BLUNT CANNULA
General Hospital
80d
Cleared
Oct 13, 1992
SUBCUTANEOUS INFUSION SET
General Hospital
251d
Cleared
Jun 04, 1991
4 LOW VOLUME IV EXTENSION SET WITH SLIDE CLAMP
General Hospital
196d
Cleared
Jun 04, 1991
4' LOW VOLUME IV EXTENSION SET
General Hospital
196d
Cleared
May 31, 1991
IV EXTENSION SETS WITH .22 MICRON FILTER
General Hospital
183d
Cleared
Oct 04, 1990
LOW VOLUME BIFURCATED IV EXTENSION SET
General Hospital
211d
Cleared
Oct 04, 1990
LOW VOLUME TRIFURCATED IV EXTENSION SET
General Hospital
211d
Cleared
Feb 28, 1990
IV BIFURCATED EXTENSION SET
General Hospital
29d
Cleared
Feb 28, 1990
IV TRIFURCATED EXTENSION SET
General Hospital
29d
Cleared
Oct 17, 1988
STRAIGHT AND RIGHT ANGLE NON-CORING NEEDLES
General Hospital
11d
Cleared
Oct 17, 1988
WINGED NON-CORING NEEDLE SET
General Hospital
11d
Cleared
Apr 29, 1988
MARQUETTE MEDICAL, INC. IV EXTENSION SETS
General Hospital
56d
Cleared
Feb 16, 1988
IV EXTENSION SET
General Hospital
56d
Cleared
Dec 30, 1987
RESERVOIR BAG
General Hospital
121d
Cleared
Dec 30, 1987
PUMP TUBING SET
General Hospital
121d