Tucker & Associates is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tucker & Associates - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Tucker & Associates has 4 FDA 510(k) cleared medical devices. Based in Sparks, US.
Historical record: 4 cleared submissions from 1997 to 2004. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Tucker & Associates Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tucker & Associates
4 devices
Cleared
Apr 26, 2004
SURGICAL FACE MASK - COLORS: WHITE, YELLOW, PINK, BLUE, AND GREEN
General Hospital
654d
Cleared
May 04, 1998
LATEX FINGER COT, POWDER-FREE, WITH PROTEIN LABELING
General Hospital
62d
Cleared
Mar 25, 1998
NITRILE EXAM GLOVE, POWDER-FREE, BLUE
General Hospital
23d
Cleared
Sep 03, 1997
FACE MASK, SURGICAL MASK, NON-STERILE
General Hospital
196d