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

Multi-Med, Inc. — Predicate Candidate Screening

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

67 daysmedian FDA review time

139 days90th percentile

7clearances measured

K-number	Device	Applicant	Decided	Review days	Recalls (K-match)
K890424	ENTERAL FEEDING CONTAINER	Multi-Med, Inc.	1989-06-14	139	0
K890396	EXTERNAL FEEDING SET FOR PUMP USE	Multi-Med, Inc.	1989-05-23	119	0
K891176	INJECTION SITE PLUG (INTRAVASCULAR ADMINISTRATION)	Multi-Med, Inc.	1989-05-18	73	0
K891919	INTRAVASCULAR ADMINISTRATION SET	Multi-Med, Inc.	1989-05-05	39	75
K891072	INTRAVASCULAR ADMINISTRATION SET	Multi-Med, Inc.	1989-04-21	51	0
K890340	INTRAVASCULAR ADMINISTRATION SET	Multi-Med, Inc.	1989-03-31	67	0
K890127	INTRAVASCULAR ADMINISTRATION SET	Multi-Med, Inc.	1989-02-03	22	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