ELECTRO-ACUPUNCTURE: ACULIFE/MODEL IDOC-01— 510(k) K091933

Name: FDA 510(k) clearance K091933
Creator: U.S. Food and Drug Administration
Published: 2010-04-02

Substantially Equivalent

Inno-Health Technology, Inc.

FDA 510(k) clearance K091933 for ELECTRO-ACUPUNCTURE: ACULIFE/MODEL IDOC-01, Substantially Equivalent on 2010-04-02. Applicant: Inno-Health Technology, Inc.. Device class: Unclassified.

Clearance details

Applicant: Inno-Health Technology, Inc.
Product code: Code BWK
Device class: Unclassified
Advisory panel: Unknown
Date received: 2009-06-30
Decision date: 2010-04-02
Decision: Substantially Equivalent
Clearance type: Special
Location: Taichung, TW

Download summary PDF View on FDA.gov ↗

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