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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K821821Substantially Equivalent

Percutaneous Tracheostomy Device

Frederic J. Toye, M.D., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K821821 is the FDA 510(k) clearance record for PERCUTANEOUS TRACHEOSTOMY DEVICE, cleared for Frederic J. Toye, M.D. on . FDA records list 6 510(k) clearances for Frederic J. Toye, M.D., from to . As of , FDA records show no recalls naming K821821.

Clearance record

Decision date
Received
(27 days to decision)
Review panel
Unknown
Applicant
Frederic J. Toye, M.D. 4221 Richmond Rd., NW, Walker MI
Third party review
No