Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
E.A. Fischione Instrument Mfg. · Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K853136 | MODEL 1100 APC(ANGIOPLASTY PRESSURE CONTROLLER) | E.A. Fischione Instrument Mfg. | 1985-12-03 | 130 | 0 |
| K841493 | MODEL 1000 APC-ANGIOPLASTY PRESSURE | E.A. Fischione Instrument Mfg. | 1984-06-11 | 62 | 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