Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Tytan Medical 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) |
|---|---|---|---|---|---|
| K092893 | TYTAN AUTOMATIC ANEROID SPHYGMOMANOMETER, MODEL A730 AND MAN | Tytan Medical Corp. | 2010-01-14 | 115 | 0 |
| K062238 | TYTAN BLOOD PRESSURE CUFF | Tytan Medical Corp. | 2006-09-21 | 50 | 0 |
| K033025 | TYTAN PROFESSIONAL /ECONOMY SERIES SPHYGMOMANOMETER, NO 710/ | Tytan Medical Corp. | 2003-12-10 | 75 | 0 |
| K023637 | TYTAN ELECTRONIC STETHOSCOPES (MODEL #600) | Tytan Medical Corp. | 2003-02-26 | 119 | 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