The following data is part of a premarket notification filed by Syva Co. with the FDA for Syva Microtrak Chlamydia Eia.
Device ID | K920503 |
510k Number | K920503 |
Device Name: | SYVA MICROTRAK CHLAMYDIA EIA |
Classification | Enzyme Linked Immunoabsorbent Assay, (chlamydiae Group) |
Applicant | SYVA CO. P.O. BOX 49013 San Jose, CA 95161 -9013 |
Contact | Rogers, Jr. |
Correspondent | Rogers, Jr. SYVA CO. P.O. BOX 49013 San Jose, CA 95161 -9013 |
Product Code | LJC |
CFR Regulation Number | 866.3120 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-02-05 |
Decision Date | 1992-09-25 |