CP Relief Wand Rx - TENS/NMES
K-Number: K252236 · 2025-08-15
Device Summary
Frequently Asked Questions
What is the CP Relief Wand Rx - TENS/NMES?
CP Relief Wand Rx - TENS/NMES is a medical device that received FDA 510(k) clearance on 2025-08-15. The listed applicant is N & C Holdings, LLC. The 510(k) number is K252236.
When did CP Relief Wand Rx - TENS/NMES receive FDA 510(k) clearance?
CP Relief Wand Rx - TENS/NMES received FDA 510(k) clearance on 2025-08-15, under 510(k) number K252236.
Who is the listed applicant for CP Relief Wand Rx - TENS/NMES?
The FDA 510(k) record lists N & C Holdings, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CP Relief Wand Rx - TENS/NMES?
The FDA product code for CP Relief Wand Rx - TENS/NMES is GZJ.
Related Devices (Code: GZJ)
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.