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FDA 510(k)

NerveTape

K-Number: K233533 · 2024-02-12

Decision Date2024-02-12
Product CodeJXI
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NerveTape is the device name listed in this FDA 510(k) record. The listed applicant is Biocircuit Technologies, Inc.. It received FDA 510(k) clearance on 2024-02-12 under 510(k) number K233533. The device is classified under product code JXI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

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

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