Antiserum, Fluorescent, Chlamydia Trachomatis
Microbiology · 21 CFR 866.3120
Recent MDR events
0 adverse event reports on file
No MDR events on file for this product code.
Event type breakdown
No data available.
Most-reported manufacturers
No data available.
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
5 firms currently registered for this product code
510(k) clearances
35 clearances for this product code
- Diagnostic Hybrids, Inc.Sep 24, 2007
K063675 · DIAGNOSTIC HYBRIDS' D3 DFA CHLAMYDIAE CULTURE CONFIRMATION KIT
- NeogenexJul 18, 1994
K941714 · CHLAMYDIA TRACHOMATIS ANTIGEN TEST
- Cel Labs Pty, Ltd.May 21, 1990
K901243 · CHLAMYDIA-CEL IMMUNOFLUORENSCENCE (IF) TEST
- Diagnostic Products Corp.Apr 16, 1990
K900870 · PATHODX CHLAMYDIA TRACHOMATIS DIRECT SPECIMEN TEST
- Diagnostic Products Corp.Feb 1, 1990
K895839 · PATHODX CHLAMYDIA CULTURE CONFIRMATION PKCC1
- Whittaker Bioproducts, Inc.Oct 6, 1988
K883352 · FLUORESCEIN CONJUGATED ANTI-CHLAMYDIA MONO ANTI
- Ortho Diagnostic Systems, Inc.Apr 27, 1988
K881500 · ORTHO* CHLAMYDIA DIRECT DETECTION (FA) TEST
- Kallestad Diag, A Div. of Erbamont, Inc.Mar 17, 1988
K880031 · PATHFINDER(TM) DIRECT DETECTION SYS C. TRACHOMATIS