The following data is part of a premarket notification filed by Immuno Probe, Inc. with the FDA for Thyroglobulin Eia Test Kit.
| Device ID | K951362 |
| 510k Number | K951362 |
| Device Name: | THYROGLOBULIN EIA TEST KIT |
| Classification | Immunochemical, Thyroglobulin Autoantibody |
| Applicant | IMMUNO PROBE, INC. COLUMBIA SQUARE 555 THIRTEENTH STREET NW Washington, DC 20004 -1109 |
| Contact | Edward C Wilson, Jr. |
| Correspondent | Edward C Wilson, Jr. IMMUNO PROBE, INC. COLUMBIA SQUARE 555 THIRTEENTH STREET NW Washington, DC 20004 -1109 |
| Product Code | JNL |
| CFR Regulation Number | 866.5870 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-03-24 |
| Decision Date | 1995-11-20 |