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FDA 510(k)

ELECTRO-ACUPUNCTURE: ACULIFE/MODEL IDOC-01

K-Number: K091933 · 2010-04-02

Decision Date2010-04-02
Product CodeBWK
DecisionSubstantially Equivalent

Device Summary

ELECTRO-ACUPUNCTURE: ACULIFE/MODEL IDOC-01 is the device name listed in this FDA 510(k) record. The listed applicant is Inno-Health Technology, Inc.. It received FDA 510(k) clearance on 2010-04-02 under 510(k) number K091933. The device is classified under product code BWK. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRO-ACUPUNCTURE: ACULIFE/MODEL IDOC-01?

ELECTRO-ACUPUNCTURE: ACULIFE/MODEL IDOC-01 is a medical device that received FDA 510(k) clearance on 2010-04-02. The listed applicant is Inno-Health Technology, Inc.. The 510(k) number is K091933.

When did ELECTRO-ACUPUNCTURE: ACULIFE/MODEL IDOC-01 receive FDA 510(k) clearance?

ELECTRO-ACUPUNCTURE: ACULIFE/MODEL IDOC-01 received FDA 510(k) clearance on 2010-04-02, under 510(k) number K091933.

Who is the listed applicant for ELECTRO-ACUPUNCTURE: ACULIFE/MODEL IDOC-01?

The FDA 510(k) record lists Inno-Health Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRO-ACUPUNCTURE: ACULIFE/MODEL IDOC-01?

The FDA product code for ELECTRO-ACUPUNCTURE: ACULIFE/MODEL IDOC-01 is BWK.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Inno-Health Technology, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: BWK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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