Zymetx, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zymetx, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Zymetx, Inc. has 4 FDA 510(k) cleared medical devices. Based in Oklahoma City, US.
Historical record: 4 cleared submissions from 1996 to 1999. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Zymetx, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Zymetx, Inc.
4 devices
Cleared
Mar 04, 1999
VIRASTAT FITC-LABELED ANTI-INFLUENZA A AND B MONOCLONAL ANTIBODIES
Microbiology
66d
Cleared
Aug 25, 1998
ZSTATFLU TEST FOR INFLUENZA TYPES A AND B VIRUSES
Microbiology
43d
Cleared
Sep 10, 1997
VIRAZYME INFLUENZA ID TEST FOR INFLUENZA TYPES A AND B VIRUSES
Microbiology
139d
Cleared
Jun 17, 1996
VIRAZYME CULTURE CONFIRMATION SCREEN FOR INFLUENZA AND PARAINFLUENZA VIRUSES
Microbiology
479d