FDA 510(k)

TES-20

K-Number: K992425 · 1999-10-19

ApplicantTes Electrical Electronic Corp.

Decision Date1999-10-19

Product CodeMWJ

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

TES-20 is the device name listed in this FDA 510(k) record. The listed applicant is Tes Electrical Electronic Corp.. It received FDA 510(k) clearance on 1999-10-19 under 510(k) number K992425. The device is classified under product code MWJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TES-20?

TES-20 is a medical device that received FDA 510(k) clearance on 1999-10-19. The listed applicant is Tes Electrical Electronic Corp.. The 510(k) number is K992425.

When did TES-20 receive FDA 510(k) clearance?

TES-20 received FDA 510(k) clearance on 1999-10-19, under 510(k) number K992425.

Who is the listed applicant for TES-20?

The FDA 510(k) record lists Tes Electrical Electronic Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TES-20?

The FDA product code for TES-20 is MWJ.

Related Devices (Code: MWJ)

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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