The following data is part of a premarket notification filed by Proto-med, Inc. with the FDA for The Emmett Iud Thread Retriever.
| Device ID | K811761 |
| 510k Number | K811761 |
| Device Name: | THE EMMETT IUD THREAD RETRIEVER |
| Classification | Remover, Intrauterine Device, Contraceptive, Hook-type |
| Applicant | PROTO-MED, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HHF |
| CFR Regulation Number | 884.4530 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-06-22 |
| Decision Date | 1981-09-21 |