510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K832477Substantially Equivalent

Oculopressor

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

K832477 is the FDA 510(k) clearance record for OCULOPRESSOR, cleared for Hans Gevder on . FDA records list one 510(k) clearance for Hans Gevder. As of , FDA records show no recalls naming K832477.

Clearance record

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