ELECTRO-ACUPUNCTURE: ACULIFE/MODEL IDOC-01
K-Number: K091933 · 2010-04-02
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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