Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Cimarron Instruments, Inc. — 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) |
|---|---|---|---|---|---|
| K840545 | PAO BIPOLAR COAGULATOR | Cimarron Instruments, Inc. | 1984-02-08 | 0 | 0 |
| K802972 | DUAL-TROL | Cimarron Instruments, Inc. | 1981-01-15 | 55 | 0 |
| K801151 | DISPOSABLE SKIN RETRACTOR | Cimarron Instruments, Inc. | 1980-05-20 | 7 | 0 |
| K790293 | CIMARRON 1000 OR 1000-2 | Cimarron Instruments, Inc. | 1979-04-12 | 63 | 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