VALTRAC (BAR) REMOVER DEVICE— 510(k) K863752

Name: FDA 510(k) clearance K863752
Creator: U.S. Food and Drug Administration
Published: 1986-10-24

Substantially Equivalent

Davis & Geck, Inc.

FDA 510(k) clearance K863752 for VALTRAC (BAR) REMOVER DEVICE, Substantially Equivalent on 1986-10-24. Applicant: Davis & Geck, Inc.. Device class: 1.

Clearance details

Applicant: Davis & Geck, Inc.
Product code: Code EMF
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1986-09-25
Decision date: 1986-10-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Danbury, CT, US

Download summary PDF View on FDA.gov ↗

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