Pain Therapy Device (Model: P.T.S-VI, P.T.S-VII)
K-Number: K231789 · 2024-03-11
ApplicantGuangzhou Xinbo Electronic Co., Ltd.
Decision Date2024-03-11
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Pain Therapy Device (Model: P.T.S-VI, P.T.S-VII) is a medical device manufactured by Guangzhou Xinbo Electronic Co., Ltd.. It received FDA 510(k) clearance on 2024-03-11 under approval number K231789. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Pain Therapy Device (Model: P.T.S-VI, P.T.S-VII)?
Pain Therapy Device (Model: P.T.S-VI, P.T.S-VII) is a medical device that received FDA 510(k) clearance on 2024-03-11. It is manufactured by Guangzhou Xinbo Electronic Co., Ltd.. The 510(k) number is K231789.
When was Pain Therapy Device (Model: P.T.S-VI, P.T.S-VII) approved by the FDA?
Pain Therapy Device (Model: P.T.S-VI, P.T.S-VII) received FDA 510(k) clearance on 2024-03-11, under approval number K231789.
What company makes Pain Therapy Device (Model: P.T.S-VI, P.T.S-VII)?
Pain Therapy Device (Model: P.T.S-VI, P.T.S-VII) is manufactured by Guangzhou Xinbo Electronic Co., Ltd..
What is the FDA product code for Pain Therapy Device (Model: P.T.S-VI, P.T.S-VII)?
The FDA product code for Pain Therapy Device (Model: P.T.S-VI, P.T.S-VII) is NGX.
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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.