K232059 is an FDA 510(k) clearance for the Tympanostomy Tubes. This device is classified as a Tube, Tympanostomy (Class II - Special Controls, product code ETD).
Submitted by Grace Medical, Inc. (Memphis, US). The FDA issued a Cleared decision on November 24, 2023, 136 days after receiving the submission on July 11, 2023.
This device falls under the Ear, Nose, Throat FDA review panel. Regulated under 21 CFR 874.3880.
| 510(k) Number | K232059 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 11, 2023 |
| Decision Date | November 24, 2023 |
| Days to Decision | 136 days |
| Submission Type | Traditional |
| Review Panel | Ear, Nose, Throat (EN) |
| Summary | Summary PDF |
| Product Code | ETD - Tube, Tympanostomy |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 874.3880 |