ELECTROSHOCK UNIT NEUROLOGY MODEL B-25— 510(k) K860467

Name: FDA 510(k) clearance K860467
Creator: U.S. Food and Drug Administration
Published: 1986-11-10

Substantially Equivalent

Medcraft Corp.

FDA 510(k) clearance K860467 for ELECTROSHOCK UNIT NEUROLOGY MODEL B-25, Substantially Equivalent on 1986-11-10. Applicant: Medcraft Corp.. Device class: 2.

Clearance details

Applicant: Medcraft Corp.
Product code: Code QGH
Device class: Class 2
Regulation: 21 CFR 882.5940
Advisory panel: Neurology
Date received: 1986-02-06
Decision date: 1986-11-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Darien, CT, US

Download summary PDF View on FDA.gov ↗

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