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
SUBSCRIBE / SIGN IN
K843829Substantially Equivalent

K-Mesh

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

K843829 is the FDA 510(k) clearance record for K-MESH, cleared for Katecho, Inc. on . FDA records list 26 510(k) clearances for Katecho, Inc., from to . As of , FDA records show no recalls naming K843829.

Clearance record

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