Device Labs, Inc. - FDA 510(k) Cleared Devices
6
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Device Labs, Inc. General Hospital ✕
5 devices
Cleared
Dec 05, 1990
CHEMOSITE IMPLANTABLE DRUG DELIVERY SYSTEM
General Hospital
69d
Cleared
Aug 01, 1990
PERCUTANEOUS INTRODUCER KIT
General Hospital
83d
Cleared
Jul 03, 1990
CHEMOSITE(TM) IMPLANTABLE DRUG DELIVERY SYSTEM
General Hospital
78d
Cleared
Dec 19, 1988
INTRAVASCULAR ADMINISTRATION SET
General Hospital
104d
Cleared
Jul 08, 1988
LO-CORE NEEDLE
General Hospital
52d