CEBOTOME DRILL— 510(k) K800275

Substantially Equivalent

American Sterilizer Co.

FDA 510(k) clearance K800275 for CEBOTOME DRILL, Substantially Equivalent on 1980-02-19. Applicant: American Sterilizer Co.. Device class: 1.

Clearance details

Applicant: American Sterilizer Co.
Product code: Code HSZ
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1980-02-07
Decision date: 1980-02-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.