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FDA 510(k)

TENS-O-TEST

K-Number: K781321 · 1978-07-31

ApplicantCuromatic, Inc.
Decision Date1978-07-31
Product Code
DecisionUnknown

Device Summary

TENS-O-TEST is the device name listed in this FDA 510(k) record. The listed applicant is Curomatic, Inc.. It received FDA 510(k) clearance on 1978-07-31 under 510(k) number K781321. FDA Decision: Unknown.

Frequently Asked Questions

What is the TENS-O-TEST?

TENS-O-TEST is a medical device that received FDA 510(k) clearance on 1978-07-31. The listed applicant is Curomatic, Inc.. The 510(k) number is K781321.

When did TENS-O-TEST receive FDA 510(k) clearance?

TENS-O-TEST received FDA 510(k) clearance on 1978-07-31, under 510(k) number K781321.

Who is the listed applicant for TENS-O-TEST?

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

Other records listing Curomatic, 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.

K791637TENS-O-TEST

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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