Atlas FDA

Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account

Alleghany Intl. Medical Technology · Predicate Candidate Screening

3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K862880SARA RTAlleghany Intl. Medical Technology1986-08-25260
K861398PRE-CHECK C02 DETECTORAlleghany Intl. Medical Technology1986-05-06210
K852062SARACAP RESPIRATORY MONITORAlleghany Intl. Medical Technology1985-08-06890

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