Needle Stimulator (Model: RJNS6-1)— 510(k) K220153

Name: FDA 510(k) clearance K220153
Creator: U.S. Food and Drug Administration
Published: 2022-03-18

Substantially Equivalent

Bozhou Rongjian Medical Appliance Co., Ltd.

FDA 510(k) clearance K220153 for Needle Stimulator (Model: RJNS6-1), Substantially Equivalent on 2022-03-18. Applicant: Bozhou Rongjian Medical Appliance Co., Ltd.. Device class: Unclassified.

Clearance details

Applicant: Bozhou Rongjian Medical Appliance Co., Ltd.
Product code: Code BWK
Device class: Unclassified
Advisory panel: Unknown
Date received: 2022-01-19
Decision date: 2022-03-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bozhou, CN

Download summary PDF View on FDA.gov ↗

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K170391 — ANSiStim-PP2017-03-09
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Data sourced from openFDA. This site is unofficial and independent of the FDA.