SCALPEL BLADE REMOVER (BLADEGARD)— 510(k) K915119

Name: FDA 510(k) clearance K915119
Creator: U.S. Food and Drug Administration
Published: 1992-05-05

Substantially Equivalent

Intergrated Visual, Inc.

FDA 510(k) clearance K915119 for SCALPEL BLADE REMOVER (BLADEGARD), Substantially Equivalent on 1992-05-05. Applicant: Intergrated Visual, Inc.. Device class: 1.

Clearance details

Applicant: Intergrated Visual, Inc.
Product code: Code GES
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1991-11-13
Decision date: 1992-05-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Quincy, IL, US

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