ANALGESIC PULSER, MODEL AP-439— 510(k) K993229

Name: FDA 510(k) clearance K993229
Creator: U.S. Food and Drug Administration
Published: 2001-02-02

Substantially Equivalent

Johari Electro-Tech Co.

FDA 510(k) clearance K993229 for ANALGESIC PULSER, MODEL AP-439, Substantially Equivalent on 2001-02-02. Applicant: Johari Electro-Tech Co.. Device class: 2.

Clearance details

Applicant: Johari Electro-Tech Co.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1999-09-27
Decision date: 2001-02-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jodhpur-342003, IN

Download summary PDF View on FDA.gov ↗

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