Evermed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Evermed, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Evermed, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1983 to 1984. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Evermed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Evermed, Inc.
6 devices
Cleared
Jul 06, 1984
STERILE HICHMAN/BROVIAC INJECTION CAP
General Hospital
133d
Cleared
Mar 12, 1984
STEIGER TUNNELING INSTRUMENT 285
Cardiovascular
33d
Cleared
Mar 01, 1983
NON-STERILE BROVIAC PARENTERAL ALIMI-
Microbiology
35d
Cleared
Mar 01, 1983
NON-STERILE CATHETER REPAIR KITS
Microbiology
22d
Cleared
Feb 28, 1983
NON-STERILE,SINGLE/SOUBLE LUMEN-CATH
General Hospital
34d
Cleared
Feb 24, 1983
NON-STERILE PERITONEAL ACCESS CATHET-
Microbiology
30d