INFANT ELECTROSURGICAL DISPERSIVE ELECTRODE— 510(k) K882421

Name: FDA 510(k) clearance K882421
Creator: U.S. Food and Drug Administration
Published: 1988-06-30

Substantially Equivalent

Dermacare Products, Inc.

FDA 510(k) clearance K882421 for INFANT ELECTROSURGICAL DISPERSIVE ELECTRODE, Substantially Equivalent on 1988-06-30. Applicant: Dermacare Products, Inc.. Device class: 2.

Clearance details

Applicant: Dermacare Products, Inc.
Product code: Code JOS
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 1988-06-13
Decision date: 1988-06-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Louisville, KT, US

Download summary PDF View on FDA.gov ↗

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