Atlas FDA

PERCUTANEOUS TRACHEOSTOMY DEVICE

FDA 510(k) clearance K821821 · decided 1982-07-19

Clearance details

K-number
K821821
Device name
PERCUTANEOUS TRACHEOSTOMY DEVICE
Applicant
Frederic J. Toye, M.D.
Decision
Substantially Equivalent
Date received
1982-06-22
Decision date
1982-07-19
Days to decision
27 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Walker, MI, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.