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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K841430Substantially Equivalent

Laserspec

Clement Clarke, Inc., Reynoldsburg OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K841430 is the FDA 510(k) clearance record for LASERSPEC, cleared for Clement Clarke, Inc. on . FDA records list 10 510(k) clearances for Clement Clarke, Inc., from to . As of , FDA records show no recalls naming K841430.

Clearance record

Decision date
Received
(251 days to decision)
Review panel
Unknown
Applicant
Clement Clarke, Inc. 6947 Americana Pkwy., Reynoldsburg OH
Third party review
No