TECNOL SILK STRIP— 510(k) K894205

Name: FDA 510(k) clearance K894205
Creator: U.S. Food and Drug Administration
Published: 1989-07-25

Substantially Equivalent

Tecnol New Jersey Wound Care, Inc.

FDA 510(k) clearance K894205 for TECNOL SILK STRIP, Substantially Equivalent on 1989-07-25. Applicant: Tecnol New Jersey Wound Care, Inc.. Device class: 1.

Clearance details

Applicant: Tecnol New Jersey Wound Care, Inc.
Product code: Code FPX
Device class: Class 1
Regulation: 21 CFR 880.5240
Advisory panel: General Hospital
Date received: 1989-06-19
Decision date: 1989-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Worth, TX, US

Download summary PDF View on FDA.gov ↗

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