Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Pryon Corp. — 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) |
|---|---|---|---|---|---|
| K942772 | A-200 MULTI-USE AIRWAY ADAPTER | Pryon Corp. | 1994-07-25 | 42 | 0 |
| K935272 | CAP 400 AT | Pryon Corp. | 1994-07-13 | 253 | 0 |
| K930250 | LOW DEAD SPACE ADAPTOR & REUASABLE AIRWAY ADAPTOR | Pryon Corp. | 1993-10-15 | 282 | 0 |
| K915773 | P-300 CAPNOGRAPH AND PULSE OXIMETER | Pryon Corp. | 1992-06-24 | 183 | 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