QI GONG MASSAGER
K-Number: K955250 · 1996-02-08
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Device Summary
Frequently Asked Questions
What is the QI GONG MASSAGER?
QI GONG MASSAGER is a medical device that received FDA 510(k) clearance on 1996-02-08. The listed applicant is East Health Development Group, Inc.. The 510(k) number is K955250.
When did QI GONG MASSAGER receive FDA 510(k) clearance?
QI GONG MASSAGER received FDA 510(k) clearance on 1996-02-08, under 510(k) number K955250.
Who is the listed applicant for QI GONG MASSAGER?
The FDA 510(k) record lists East Health Development Group, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QI GONG MASSAGER?
The FDA product code for QI GONG MASSAGER is IRO.
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.
Related Devices (Code: IRO)
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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