TBD TENS REUSABLE ELECTRODE
K-Number: K902195 · 1990-06-08
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Device Summary
Frequently Asked Questions
What is the TBD TENS REUSABLE ELECTRODE?
TBD TENS REUSABLE ELECTRODE is a medical device that received FDA 510(k) clearance on 1990-06-08. The listed applicant is Empi. The 510(k) number is K902195.
When did TBD TENS REUSABLE ELECTRODE receive FDA 510(k) clearance?
TBD TENS REUSABLE ELECTRODE received FDA 510(k) clearance on 1990-06-08, under 510(k) number K902195.
Who is the listed applicant for TBD TENS REUSABLE ELECTRODE?
The FDA 510(k) record lists Empi as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TBD TENS REUSABLE ELECTRODE?
The FDA product code for TBD TENS REUSABLE ELECTRODE 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 Empi 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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