PRODUCT LINE-COMBO STIMULATOR/SEQUENTIAL STIMULATOR, MODEL IF-5000— 510(k) K024036

Name: FDA 510(k) clearance K024036
Creator: U.S. Food and Drug Administration
Published: 2002-12-20

Substantially Equivalent

Johari Digital Healthcare , Ltd.

FDA 510(k) clearance K024036 for PRODUCT LINE-COMBO STIMULATOR/SEQUENTIAL STIMULATOR, MODEL IF-5000, Substantially Equivalent on 2002-12-20. Applicant: Johari Digital Healthcare , Ltd.. Device class: 2.

Clearance details

Applicant: Johari Digital Healthcare , Ltd.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2002-12-06
Decision date: 2002-12-20
Decision: Substantially Equivalent
Clearance type: Special
Location: Jodhpur, Raj, IN

Download summary PDF View on FDA.gov ↗

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