510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K842371Substantially Equivalent

Lee Syringe

Peter F. Lee, Inc., Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K842371 is the FDA 510(k) clearance record for LEE SYRINGE, cleared for Peter F. Lee, Inc. on . FDA records list one 510(k) clearance for Peter F. Lee, Inc. As of , FDA records show no recalls naming K842371.

Clearance record

Decision date
Received
(213 days to decision)
Review panel
Unknown
Applicant
Peter F. Lee, Inc. 5200 W. 73rd., Minneapolis MN
Third party review
No