Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Micron Instruments, Inc. — Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K843488 | ELECTROSTIM 380 | Micron Instruments, Inc. | 1984-09-19 | 13 | 0 |
| K822924 | MINISTIM 180 | Micron Instruments, Inc. | 1982-12-13 | 73 | 0 |
| K810044 | MUSCLE STIMULATOR | Micron Instruments, Inc. | 1981-02-26 | 49 | 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