Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Beecher Medical Diagnostic Instrumentation · 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) |
|---|---|---|---|---|---|
| K871830 | NAPSAC(TM) | Beecher Medical Diagnostic Instrumentation | 1987-09-09 | 121 | 0 |
| K850288 | HEPATIC PARENCHYMAL SUCTION DISSECTOR | Beecher Medical Diagnostic Instrumentation | 1985-03-18 | 53 | 0 |
| K833800 | BEECHER 20 GA. PROBE | Beecher Medical Diagnostic Instrumentation | 1984-01-04 | 65 | 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