NerveTape
K-Number: K233533 · 2024-02-12
Device Summary
Frequently Asked Questions
What is the NerveTape?
NerveTape is a medical device that received FDA 510(k) clearance on 2024-02-12. The listed applicant is Biocircuit Technologies, Inc.. The 510(k) number is K233533.
When did NerveTape receive FDA 510(k) clearance?
NerveTape received FDA 510(k) clearance on 2024-02-12, under 510(k) number K233533.
Who is the listed applicant for NerveTape?
The FDA 510(k) record lists Biocircuit Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NerveTape?
The FDA product code for NerveTape is JXI.
Other records listing Biocircuit Technologies, 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: JXI)
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.