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FDA 510(k)

TENS CONDUCTIVE MEDIA PAD

K-Number: K904889 · 1991-05-14

ApplicantCreative Design Systems, Inc.
Decision Date1991-05-14
Product CodeGYB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TENS CONDUCTIVE MEDIA PAD is the device name listed in this FDA 510(k) record. The listed applicant is Creative Design Systems, Inc.. It received FDA 510(k) clearance on 1991-05-14 under 510(k) number K904889. The device is classified under product code GYB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TENS CONDUCTIVE MEDIA PAD?

TENS CONDUCTIVE MEDIA PAD is a medical device that received FDA 510(k) clearance on 1991-05-14. The listed applicant is Creative Design Systems, Inc.. The 510(k) number is K904889.

When did TENS CONDUCTIVE MEDIA PAD receive FDA 510(k) clearance?

TENS CONDUCTIVE MEDIA PAD received FDA 510(k) clearance on 1991-05-14, under 510(k) number K904889.

Who is the listed applicant for TENS CONDUCTIVE MEDIA PAD?

The FDA 510(k) record lists Creative Design Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TENS CONDUCTIVE MEDIA PAD?

The FDA product code for TENS CONDUCTIVE MEDIA PAD is GYB.

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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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