The following data is part of a premarket notification filed by Micromedic Systems with the FDA for Autopak-12 Uptake Test Delivery System.
| Device ID | K792662 |
| 510k Number | K792662 |
| Device Name: | AUTOPAK-12 UPTAKE TEST DELIVERY SYSTEM |
| Classification | Radioassay, Triiodothyronine Uptake |
| Applicant | MICROMEDIC SYSTEMS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KHQ |
| CFR Regulation Number | 862.1715 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-12-26 |
| Decision Date | 1980-01-17 |