Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ANSiStim-PP

K-Number: K170391 · 2017-03-09

ApplicantDyansys, Inc.
Decision Date2017-03-09
Product CodeBWK
DecisionSubstantially Equivalent

Device Summary

ANSiStim-PP is a medical device manufactured by Dyansys, Inc.. It received FDA 510(k) clearance on 2017-03-09 under approval number K170391. The device is classified under product code BWK. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANSiStim-PP?

ANSiStim-PP is a medical device that received FDA 510(k) clearance on 2017-03-09. It is manufactured by Dyansys, Inc.. The 510(k) number is K170391.

When was ANSiStim-PP approved by the FDA?

ANSiStim-PP received FDA 510(k) clearance on 2017-03-09, under approval number K170391.

What company makes ANSiStim-PP?

ANSiStim-PP is manufactured by Dyansys, Inc..

What is the FDA product code for ANSiStim-PP?

The FDA product code for ANSiStim-PP is BWK.

Other Devices by Dyansys, Inc.

K173861Drug Relief K202940First Relief v1 K212859First Relief K211971Drug Relief v1 K221425Primary Relief K221231Drug Relief v1

View all 9 devices →

Related Devices (Code: BWK)

K152571StivaxBiegler GmbH K202861Needle StimulatorWuxi Jiajian Medical Instrument Co., Ltd. K200636AXUS ES-5 Electro-Acupuncture DeviceLhasa Oms, Inc. K220153Needle Stimulator (Model: RJNS6-1)Bozhou Rongjian Medical Appliance Co., Ltd. K244030Needle Stimulator (CMNS6-1 PLUS, CMNS6-3)Wuxi Jiajian Medical Instrument Co., Ltd.

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.

↑