Virion (U.S.), Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Virion (U.S.), Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Virion (U.S.), Inc. has 5 FDA 510(k) cleared medical devices. Based in Morristown, US.
Historical record: 5 cleared submissions from 1987 to 1994. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Virion (U.S.), Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Virion (U.S.), Inc.
5 devices
Cleared
Jun 13, 1994
EPSTEIN-BARR VIRUS COMBI TEST, EBV COMBI TEST
Microbiology
346d
Cleared
Jun 29, 1992
COXSACKIE VIRUS B1-B6 CF ANTIGENS
Microbiology
84d
Cleared
Jun 17, 1991
MUMPS COMPLEMENT-FIXATION (C.F.) ANTIGEN
Microbiology
201d
Cleared
Mar 21, 1991
P.I.V. COMPLEMENT-FIXATION (C.F.) ANTIGEN
Microbiology
111d
Cleared
Oct 30, 1987
TOXOPLASMA GONDII
Microbiology
312d