AXICUT DISPOSABLE SCALPEL— 510(k) K811707

Substantially Equivalent

Neonatal Corp.

FDA 510(k) clearance K811707 for AXICUT DISPOSABLE SCALPEL, Substantially Equivalent on 1981-07-20. Applicant: Neonatal Corp.. Device class: 1.

Clearance details

Applicant: Neonatal Corp.
Product code: Code GDX
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1981-06-16
Decision date: 1981-07-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Neonatal Corp.

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