510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K770879Substantially Equivalent

Bronchofiberscope, Fb-19A

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

K770879 is the FDA 510(k) clearance record for BRONCHOFIBERSCOPE, FB-19A, 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 K770879.

Clearance record

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