PROFORE FOUR-LAYER BANDAGE SYSTEM KIT— 510(k) K961775

Name: FDA 510(k) clearance K961775
Creator: U.S. Food and Drug Administration
Published: 1996-07-16

Substantially Equivalent

Smith & Nephew United, Inc.

FDA 510(k) clearance K961775 for PROFORE FOUR-LAYER BANDAGE SYSTEM KIT, Substantially Equivalent on 1996-07-16. Applicant: Smith & Nephew United, Inc.. Device class: Unclassified.

Clearance details

Applicant: Smith & Nephew United, Inc.
Product code: Code EFQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1996-05-08
Decision date: 1996-07-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Largo, FL, US

Download summary PDF View on FDA.gov ↗

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