Gempco, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gempco, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Gempco, Inc. has 4 FDA 510(k) cleared medical devices. Based in Lisle, US.
Historical record: 4 cleared submissions from 1988 to 1988. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Gempco, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gempco, Inc.
4 devices
Cleared
Dec 22, 1988
MODEL WC-102 NEWBORN BED & EQUIPMENT CABINET
General Hospital
71d
Cleared
Dec 22, 1988
MODEL WC-107 MOBILE NEWBORN BED
General Hospital
71d
Cleared
Dec 22, 1988
MODEL WC-115 MOBILE BASSINET
General Hospital
71d
Cleared
Jul 12, 1988
SPECIAL PROCEDURES BASE UNIT MODEL 500
General Hospital
82d