DEBUTRON— 510(k) K782119

Substantially Equivalent

Martin Electric Co.

FDA 510(k) clearance K782119 for DEBUTRON, Substantially Equivalent on 1979-02-26. Applicant: Martin Electric Co.. Device class: 1.

Clearance details

Applicant: Martin Electric Co.
Product code: Code KCX
Device class: Class 1
Regulation: 21 CFR 878.5360
Advisory panel: General, Plastic Surgery
Date received: 1978-12-27
Decision date: 1979-02-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KCX

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K973179 — FEMINIQUE SONIC HAIR REMOVER1997-10-30
K972695 — FINALLY FREE1997-10-22

Data sourced from openFDA. This site is unofficial and independent of the FDA.