STERILE INSTRUMENT DRAPE— 510(k) K902763

Name: FDA 510(k) clearance K902763
Creator: U.S. Food and Drug Administration
Published: 1990-09-20

Substantially Equivalent

North American Sterilization & Packaging Co.

FDA 510(k) clearance K902763 for STERILE INSTRUMENT DRAPE, Substantially Equivalent on 1990-09-20. Applicant: North American Sterilization & Packaging Co.. Device class: 2.

Clearance details

Applicant: North American Sterilization & Packaging Co.
Product code: Code HMW
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1990-06-25
Decision date: 1990-09-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sparta, NJ, 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.