LANCE LTD. STERI. STITCH CUTTER BLADE— 510(k) K770217

Name: FDA 510(k) clearance K770217
Creator: U.S. Food and Drug Administration
Published: 1977-03-30

Substantially Equivalent

Aeroceuticals

FDA 510(k) clearance K770217 for LANCE LTD. STERI. STITCH CUTTER BLADE, Substantially Equivalent on 1977-03-30. Applicant: Aeroceuticals. Device class: 1.

Clearance details

Applicant: Aeroceuticals
Product code: Code GES
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1977-02-02
Decision date: 1977-03-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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