Dms Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dms Products, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Dms Products, Inc. has 6 FDA 510(k) cleared medical devices. Based in Flemington, US.
Historical record: 6 cleared submissions from 1986 to 1989. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Dms Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dms Products, Inc.
6 devices
Cleared
Nov 09, 1989
RAPIDEC STAPH
Microbiology
254d
Cleared
Sep 26, 1989
RAPIDEC UR
Microbiology
60d
Cleared
Jun 02, 1989
RAPIDEC COLI
Microbiology
115d
Cleared
Feb 17, 1989
JAMES REAGENT
Microbiology
10d
Cleared
Mar 06, 1986
API 20 EC (ENTEROBACTERIACEAE)(IDENTIFICATION KIT)
Microbiology
101d
Cleared
Mar 04, 1986
API 50 CHB (CULTURE MEDIA)
Microbiology
99d