Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Mallinckrodt Anesthesia Products · Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K912240CPAP SYSTEM AND BRONCHO-CATH W/CPAP SYSTEMMallinckrodt Anesthesia Products1991-08-22930
K895875MODEL 4070 TEMPERATURE MONITORMallinckrodt Anesthesia Products1989-12-21780
K890484HI-LO TEMP GENERAL PURPOSE TEMPERATURE PROBEMallinckrodt Anesthesia Products1989-04-21800

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