The following data is part of a premarket notification filed by Inova Diagnostics, Inc. with the FDA for Quanta Lite Ccp3.1 Igg/iga Elisa.
| Device ID | K072944 |
| 510k Number | K072944 |
| Device Name: | QUANTA LITE CCP3.1 IGG/IGA ELISA |
| Classification | Antibodies, Anti-cyclic Citrullinated Peptide (ccp) |
| Applicant | INOVA DIAGNOSTICS, INC. 9900 OLD GROVE RD. San Diego, CA 92131 -1638 |
| Contact | Rufus Burlingame |
| Correspondent | Rufus Burlingame INOVA DIAGNOSTICS, INC. 9900 OLD GROVE RD. San Diego, CA 92131 -1638 |
| Product Code | NHX |
| CFR Regulation Number | 866.5775 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-10-17 |
| Decision Date | 2008-03-05 |