TENS device-EmeTerm, CinvStop
K-Number: K172478 · 2018-04-19
Decision Date2018-04-19
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
TENS device-EmeTerm, CinvStop is a medical device manufactured by Wat Medical Technology (Ningbo) Co., Ltd.. It received FDA 510(k) clearance on 2018-04-19 under approval number K172478. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the TENS device-EmeTerm, CinvStop?
TENS device-EmeTerm, CinvStop is a medical device that received FDA 510(k) clearance on 2018-04-19. It is manufactured by Wat Medical Technology (Ningbo) Co., Ltd.. The 510(k) number is K172478.
When was TENS device-EmeTerm, CinvStop approved by the FDA?
TENS device-EmeTerm, CinvStop received FDA 510(k) clearance on 2018-04-19, under approval number K172478.
What company makes TENS device-EmeTerm, CinvStop?
TENS device-EmeTerm, CinvStop is manufactured by Wat Medical Technology (Ningbo) Co., Ltd..
What is the FDA product code for TENS device-EmeTerm, CinvStop?
The FDA product code for TENS device-EmeTerm, CinvStop is GZJ.
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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.