WIREDRIVER— 510(k) K772324

Substantially Equivalent

American Sterilizer Co.

FDA 510(k) clearance K772324 for WIREDRIVER, Substantially Equivalent on 1978-01-03. 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: 1977-12-19
Decision date: 1978-01-03
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.