Immunetics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Immunetics, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Immunetics, Inc. has 4 FDA 510(k) cleared medical devices. Based in Cambridge,, US.
Historical record: 4 cleared submissions from 1999 to 2004. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Immunetics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Immunetics, Inc.
4 devices
Cleared
Jun 03, 2004
QUICKELISA ANTHRAX-PA KIT
Microbiology
107d
Cleared
May 10, 2001
IMMUNETICS C6 LYME ELISA KIT
Microbiology
156d
Cleared
Sep 21, 1999
QUALICODE B. BURGDORFERI IGM WESTERN BLOT KIT, MODEL DK-C062-024
Microbiology
174d
Cleared
Sep 21, 1999
QUALICODE B. BURGDORFERI IGG WESTERN BLOT KIT, MODEL DK-C052-024
Microbiology
174d