510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K761141Substantially Equivalent

Arterial Graft Sizers

Pilling Co., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K761141 is the FDA 510(k) clearance record for ARTERIAL GRAFT SIZERS, cleared for Pilling Co. on . FDA records list 40 510(k) clearances for Pilling Co., from to . As of , FDA records show no recalls naming K761141.

Clearance record

Decision date
Received
(41 days to decision)
Review panel
Unknown
Applicant
Pilling Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No