MSB TENS ELECTRODES (DISPOSABLE)
K-Number: K980229 · 1998-02-27
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Device Summary
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.
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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