The following data is part of a premarket notification filed by The Binding Site Ltd. with the FDA for Igd Diagnostic Test Kits.
| Device ID | K051299 |
| 510k Number | K051299 |
| Device Name: | IGD DIAGNOSTIC TEST KITS |
| Classification | Igd, Antigen, Antiserum, Control |
| Applicant | THE BINDING SITE LTD. 2425 WEST OLYMPIC BOULEVARD WEST TOWER, SUITE 4000 Santa Monica, CA 90404 |
| Contact | Jay H Geller |
| Correspondent | Jay H Geller THE BINDING SITE LTD. 2425 WEST OLYMPIC BOULEVARD WEST TOWER, SUITE 4000 Santa Monica, CA 90404 |
| Product Code | CZJ |
| CFR Regulation Number | 866.5510 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-05-18 |
| Decision Date | 2005-11-23 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 05051700006255 | K051299 | 000 |