The following data is part of a premarket notification filed by Biomerieux Vitek, Inc. with the FDA for Vidas Toxo Competition (txc) Assay.
Device ID | K931334 |
510k Number | K931334 |
Device Name: | VIDAS TOXO COMPETITION (TXC) ASSAY |
Classification | Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii |
Applicant | BIOMERIEUX VITEK, INC. 1022 HINGHAM ST. Rockland, MA 02370 |
Contact | Vicki Anastasi |
Correspondent | Vicki Anastasi BIOMERIEUX VITEK, INC. 1022 HINGHAM ST. Rockland, MA 02370 |
Product Code | LGD |
CFR Regulation Number | 866.3780 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-03-16 |
Decision Date | 1993-06-21 |