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FDA 510(k)

MSB TENS ELECTRODES (DISPOSABLE)

K-Number: K980229 · 1998-02-27

ApplicantMsb , Ltd.
Decision Date1998-02-27
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MSB TENS ELECTRODES (DISPOSABLE) is the device name listed in this FDA 510(k) record. The listed applicant is Msb , Ltd.. It received FDA 510(k) clearance on 1998-02-27 under 510(k) number K980229. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MSB TENS ELECTRODES (DISPOSABLE)?

MSB TENS ELECTRODES (DISPOSABLE) is a medical device that received FDA 510(k) clearance on 1998-02-27. The listed applicant is Msb , Ltd.. The 510(k) number is K980229.

When did MSB TENS ELECTRODES (DISPOSABLE) receive FDA 510(k) clearance?

MSB TENS ELECTRODES (DISPOSABLE) received FDA 510(k) clearance on 1998-02-27, under 510(k) number K980229.

Who is the listed applicant for MSB TENS ELECTRODES (DISPOSABLE)?

The FDA 510(k) record lists Msb , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MSB TENS ELECTRODES (DISPOSABLE)?

The FDA product code for MSB TENS ELECTRODES (DISPOSABLE) is GXY.

Related Clinical Trials

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.

Other records listing Msb , Ltd. 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.

View all 7 devices →

Related Devices (Code: GXY)

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.

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