ANSiStim-PP
K-Number: K170391 · 2017-03-09
Device Summary
Frequently Asked Questions
What is the ANSiStim-PP?
ANSiStim-PP is a medical device that received FDA 510(k) clearance on 2017-03-09. The listed applicant is Dyansys, Inc.. The 510(k) number is K170391.
When did ANSiStim-PP receive FDA 510(k) clearance?
ANSiStim-PP received FDA 510(k) clearance on 2017-03-09, under 510(k) number K170391.
Who is the listed applicant for ANSiStim-PP?
The FDA 510(k) record lists Dyansys, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANSiStim-PP?
The FDA product code for ANSiStim-PP is BWK.
Other records listing Dyansys, Inc. as applicant
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: BWK)
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.