I.V. SUPPORT, TECNOL ARMBOARD— 510(k) K760308

Name: FDA 510(k) clearance K760308
Creator: U.S. Food and Drug Administration
Published: 1976-08-11

Substantially Equivalent

Tecnol New Jersey Wound Care, Inc.

FDA 510(k) clearance K760308 for I.V. SUPPORT, TECNOL ARMBOARD, Substantially Equivalent on 1976-08-11. Applicant: Tecnol New Jersey Wound Care, Inc.. Device class: 1.

Clearance details

Applicant: Tecnol New Jersey Wound Care, Inc.
Product code: Code FSE
Device class: Class 1
Regulation: 21 CFR 878.4950
Advisory panel: General, Plastic Surgery
Date received: 1976-07-26
Decision date: 1976-08-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hammonton, NJ, US

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