The following data is part of a premarket notification filed by Exmoor Plastics Ltd. with the FDA for Exmoor Aural Grommet Ag/ti.
| Device ID | K812459 |
| 510k Number | K812459 |
| Device Name: | EXMOOR AURAL GROMMET AG/TI |
| Classification | Tube, Tympanostomy |
| Applicant | EXMOOR PLASTICS LTD. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | ETD |
| CFR Regulation Number | 874.3880 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-08-31 |
| Decision Date | 1981-09-25 |