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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K823075Substantially Equivalent

Rexton

Argosy Intl. (USA), Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K823075 is the FDA 510(k) clearance record for REXTON, cleared for Argosy Intl. (Usa), Inc. on . FDA records list 14 510(k) clearances for Argosy Intl. (Usa), Inc., from to . As of , FDA records show no recalls naming K823075.

Clearance record

Decision date
Received
(20 days to decision)
Review panel
Unknown
Applicant
Argosy Intl. (Usa), Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No