Regent Hospital Products is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Regent Hospital Products - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Regent Hospital Products has 5 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 5 cleared submissions from 1989 to 1995. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Regent Hospital Products Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Regent Hospital Products
5 devices
Cleared
Sep 01, 1995
REGENT BIOGEL LATEX-FREE SURGEON'S GLOVE
General Hospital
130d
Cleared
Jun 13, 1991
RUBBER LATEX SURGEONS GLOVES
General Hospital
100d
Cleared
Aug 10, 1990
REGENT BIOGEL DIAG PROCED GLOVES HYPOALLERG CLAIMS
General Hospital
59d
Cleared
Feb 01, 1990
RUBBER LATEX SURGEON'S GLOVE
General Hospital
85d
Cleared
Jun 06, 1989
REGENT BIOGEL D(TM) NON-STERILE DENTAL GLOVES
General Hospital
78d