510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
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K832405Substantially Equivalent

Opthalmic Endoscope

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

K832405 is the FDA 510(k) clearance record for OPTHALMIC ENDOSCOPE, cleared for Cilco, Inc. on . FDA records list 6 510(k) clearances for Cilco, Inc., from to . As of , FDA records show no recalls naming K832405.

Clearance record

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