Atlas FDA

CUI CHIN SIZER

FDA 510(k) clearance K854339 · decided 1985-11-15

Clearance details

K-number
K854339
Device name
CUI CHIN SIZER
Applicant
Cox-Uphuff Intl.
Decision
Substantially Equivalent
Date received
1985-10-28
Decision date
1985-11-15
Days to decision
18 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Santa Barbara, CA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.