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FDA 510(k)

MODIFIED ISLAND TENS DISP. ELECTRODE FOR SNAP CONN

K-Number: K896485 · 1989-12-21

ApplicantEmpi
Decision Date1989-12-21
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MODIFIED ISLAND TENS DISP. ELECTRODE FOR SNAP CONN is the device name listed in this FDA 510(k) record. The listed applicant is Empi. It received FDA 510(k) clearance on 1989-12-21 under 510(k) number K896485. 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 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.

View all 60 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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