INTERDRY SILVER— 510(k) K110715

Name: FDA 510(k) clearance K110715
Creator: U.S. Food and Drug Administration
Published: 2011-11-04

Substantially Equivalent

Milliken Healthcare Products, LLC

FDA 510(k) clearance K110715 for INTERDRY SILVER, Substantially Equivalent on 2011-11-04. Applicant: Milliken Healthcare Products, LLC. Device class: 1.

Clearance details

Applicant: Milliken Healthcare Products, LLC
Product code: Code FRL
Device class: Class 1
Regulation: 21 CFR 880.5300
Advisory panel: General Hospital
Date received: 2011-03-15
Decision date: 2011-11-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Spartanburg, SC, US

Download summary PDF View on FDA.gov ↗

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