Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Muskogee Regional Hearing Aid Lab · Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K950963 | AUDIOTECH MODEL SPI | Muskogee Regional Hearing Aid Lab | 1995-05-25 | 84 | 0 |
| K931975 | AUDIOTECH MODEL DP | Muskogee Regional Hearing Aid Lab | 1993-06-22 | 61 | 0 |
| K903479 | AUDIOTECH MODEL DB | Muskogee Regional Hearing Aid Lab | 1990-10-09 | 68 | 0 |
| K903478 | AUDIOTECH MODEL CL | Muskogee Regional Hearing Aid Lab | 1990-10-09 | 68 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda