Pain Therapy Device(Model: P.T.S-X)
K-Number: K230711 · 2024-05-16
ApplicantGuangzhou Xinbo Electronic Co., Ltd.
Decision Date2024-05-16
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Pain Therapy Device(Model: P.T.S-X) is a medical device manufactured by Guangzhou Xinbo Electronic Co., Ltd.. It received FDA 510(k) clearance on 2024-05-16 under approval number K230711. 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-X)?
Pain Therapy Device(Model: P.T.S-X) is a medical device that received FDA 510(k) clearance on 2024-05-16. It is manufactured by Guangzhou Xinbo Electronic Co., Ltd.. The 510(k) number is K230711.
When was Pain Therapy Device(Model: P.T.S-X) approved by the FDA?
Pain Therapy Device(Model: P.T.S-X) received FDA 510(k) clearance on 2024-05-16, under approval number K230711.
What company makes Pain Therapy Device(Model: P.T.S-X)?
Pain Therapy Device(Model: P.T.S-X) is manufactured by Guangzhou Xinbo Electronic Co., Ltd..
What is the FDA product code for Pain Therapy Device(Model: P.T.S-X)?
The FDA product code for Pain Therapy Device(Model: P.T.S-X) 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.