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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K841652Substantially Equivalent

Ocular Pressure Applicator

The Lebanon Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K841652 is the FDA 510(k) clearance record for OCULAR PRESSURE APPLICATOR, cleared for The Lebanon Corp. on . FDA records list 3 510(k) clearances for The Lebanon Corp., from to . As of , FDA records show no recalls naming K841652.

Clearance record

Decision date
Received
(42 days to decision)
Review panel
Unknown
Applicant
The Lebanon Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No