FDA 510(k)

TENS LEAD

K-Number: K873608 · 1987-09-30

Decision Date1987-09-30

Product CodeGZI

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

TENS LEAD is the device name listed in this FDA 510(k) record. The listed applicant is Desco Industries, Inc.. It received FDA 510(k) clearance on 1987-09-30 under 510(k) number K873608. The device is classified under product code GZI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TENS LEAD?

TENS LEAD is a medical device that received FDA 510(k) clearance on 1987-09-30. The listed applicant is Desco Industries, Inc.. The 510(k) number is K873608.

When did TENS LEAD receive FDA 510(k) clearance?

TENS LEAD received FDA 510(k) clearance on 1987-09-30, under 510(k) number K873608.

Who is the listed applicant for TENS LEAD?

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

What is the FDA product code for TENS LEAD?

The FDA product code for TENS LEAD is GZI.

Other records listing Desco Industries, Inc. 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.

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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.