MSI SURGICAL DRAPES— 510(k) K974672

Name: FDA 510(k) clearance K974672
Creator: U.S. Food and Drug Administration
Published: 1998-03-13

Substantially Equivalent

Medical Specialty Innovations, Inc. (Msi)

FDA 510(k) clearance K974672 for MSI SURGICAL DRAPES, Substantially Equivalent on 1998-03-13. Applicant: Medical Specialty Innovations, Inc. (Msi). Device class: 2.

Clearance details

Applicant: Medical Specialty Innovations, Inc. (Msi)
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1997-12-15
Decision date: 1998-03-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, US

Download summary PDF View on FDA.gov ↗

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