MODIFIED ISLAND TENS DISP. ELECTRODE FOR SNAP CONN
K-Number: K896485 · 1989-12-21
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Device Summary
Frequently Asked Questions
What is the MODIFIED ISLAND TENS DISP. ELECTRODE FOR SNAP CONN?
MODIFIED ISLAND TENS DISP. ELECTRODE FOR SNAP CONN is a medical device that received FDA 510(k) clearance on 1989-12-21. The listed applicant is Empi. The 510(k) number is K896485.
When did MODIFIED ISLAND TENS DISP. ELECTRODE FOR SNAP CONN receive FDA 510(k) clearance?
MODIFIED ISLAND TENS DISP. ELECTRODE FOR SNAP CONN received FDA 510(k) clearance on 1989-12-21, under 510(k) number K896485.
Who is the listed applicant for MODIFIED ISLAND TENS DISP. ELECTRODE FOR SNAP CONN?
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 MODIFIED ISLAND TENS DISP. ELECTRODE FOR SNAP CONN?
The FDA product code for MODIFIED ISLAND TENS DISP. ELECTRODE FOR SNAP CONN 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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