KLINIDRAPE SURGICAL DRAPES— 510(k) K031131

Name: FDA 510(k) clearance K031131
Creator: U.S. Food and Drug Administration
Published: 2003-06-10

Substantially Equivalent

Molnlycke Health Care

FDA 510(k) clearance K031131 for KLINIDRAPE SURGICAL DRAPES, Substantially Equivalent on 2003-06-10. Applicant: Molnlycke Health Care. Device class: 2.

Clearance details

Applicant: Molnlycke Health Care
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 2003-04-09
Decision date: 2003-06-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newton, PA, US

Download summary PDF View on FDA.gov ↗

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