The following data is part of a premarket notification filed by Ciba Corning Diagnostics Corp. with the FDA for Ciba Corning Magic Lite Chlamydia Immunoassay.
Device ID | K902270 |
510k Number | K902270 |
Device Name: | CIBA CORNING MAGIC LITE CHLAMYDIA IMMUNOASSAY |
Classification | Enzyme Linked Immunoabsorbent Assay, (chlamydiae Group) |
Applicant | CIBA CORNING DIAGNOSTICS CORP. 333 CONEY ST. E. Walpole, MA 02032 |
Contact | J Pignato |
Correspondent | J Pignato CIBA CORNING DIAGNOSTICS CORP. 333 CONEY ST. E. Walpole, MA 02032 |
Product Code | LJC |
CFR Regulation Number | 866.3120 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-05-21 |
Decision Date | 1990-07-31 |