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FDA 510(k)

TENS DEVICE FOR RELIEF OF CHRONIC PAIN, MODIFIED

K-Number: K924876 · 1994-03-01

ApplicantGraham-Field, Inc.
Decision Date1994-03-01
Product CodeGZT
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TENS DEVICE FOR RELIEF OF CHRONIC PAIN, MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Graham-Field, Inc.. It received FDA 510(k) clearance on 1994-03-01 under 510(k) number K924876. The device is classified under product code GZT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TENS DEVICE FOR RELIEF OF CHRONIC PAIN, MODIFIED?

TENS DEVICE FOR RELIEF OF CHRONIC PAIN, MODIFIED is a medical device that received FDA 510(k) clearance on 1994-03-01. The listed applicant is Graham-Field, Inc.. The 510(k) number is K924876.

When did TENS DEVICE FOR RELIEF OF CHRONIC PAIN, MODIFIED receive FDA 510(k) clearance?

TENS DEVICE FOR RELIEF OF CHRONIC PAIN, MODIFIED received FDA 510(k) clearance on 1994-03-01, under 510(k) number K924876.

Who is the listed applicant for TENS DEVICE FOR RELIEF OF CHRONIC PAIN, MODIFIED?

The FDA 510(k) record lists Graham-Field, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TENS DEVICE FOR RELIEF OF CHRONIC PAIN, MODIFIED?

The FDA product code for TENS DEVICE FOR RELIEF OF CHRONIC PAIN, MODIFIED is GZT.

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Other records listing Graham-Field, Inc. as applicant

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Related Devices (Code: GZT)

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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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