510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K822554Substantially Equivalent

Cement Extraction Instrumentation

Surgi-Quip Inc.U, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K822554 is the FDA 510(k) clearance record for CEMENT EXTRACTION INSTRUMENTATION, cleared for Surgi-Quip Inc.U on . FDA records list 8 510(k) clearances for Surgi-Quip Inc.U, from to . As of , FDA records show no recalls naming K822554.

Clearance record

Decision date
Received
(21 days to decision)
Review panel
Unknown
Applicant
Surgi-Quip Inc.U 803 N. Front St. Suite 3, Mchenry IL
Third party review
No