Carrom Healthcare, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Carrom Healthcare, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Carrom Healthcare, Inc. has 5 FDA 510(k) cleared medical devices. Based in St. Louis, US.
Historical record: 5 cleared submissions from 1985 to 1986. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Carrom Healthcare, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Carrom Healthcare, Inc.
5 devices
Cleared
Feb 04, 1986
EVEREST & JENNING SERIES 5000 MODULAR BED
General Hospital
63d
Cleared
Feb 04, 1986
EVEREST & JENNINGS TRADITION-STANDARD BED L109684&
General Hospital
61d
Cleared
Feb 04, 1986
CARROM CARELIFE SERIES 40000 MODULAR BES SYSTEM
General Hospital
56d
Cleared
Dec 13, 1985
EVEREST & JENNINGS BED MODEL NO. L109564 & L108564
General Hospital
14d
Cleared
Nov 13, 1985
CENTERCOM CONTROL
General Hospital
100d