The following data is part of a premarket notification filed by The Binding Site Group Ltd with the FDA for The Optilite Igg3 Kit.
| Device ID | K142735 |
| 510k Number | K142735 |
| Device Name: | The Optilite IgG3 Kit |
| Classification | Method, Nephelometric, Immunoglobulins (g, A, M) |
| Applicant | THE BINDING SITE GROUP LTD 8 CALTHORPE ROAD, EDGBASTON Birmingham, GB B15 1qt |
| Contact | Andrea Thomas |
| Correspondent | Andrea Thomas THE BINDING SITE GROUP LTD 8 CALTHORPE ROAD, EDGBASTON Birmingham, GB B15 1qt |
| Product Code | CFN |
| CFR Regulation Number | 866.5510 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-09-23 |
| Decision Date | 2014-12-21 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 05051700017541 | K142735 | 000 |