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FDA 510(k)

T-METER

K-Number: K840487 · 1984-03-12

ApplicantK.J. Electronics
Decision Date1984-03-12
Product CodeHCS
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

T-METER is the device name listed in this FDA 510(k) record. The listed applicant is K.J. Electronics. It received FDA 510(k) clearance on 1984-03-12 under 510(k) number K840487. The device is classified under product code HCS. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the T-METER?

T-METER is a medical device that received FDA 510(k) clearance on 1984-03-12. The listed applicant is K.J. Electronics. The 510(k) number is K840487.

When did T-METER receive FDA 510(k) clearance?

T-METER received FDA 510(k) clearance on 1984-03-12, under 510(k) number K840487.

Who is the listed applicant for T-METER?

The FDA 510(k) record lists K.J. Electronics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for T-METER?

The FDA product code for T-METER is HCS.

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Related Devices (Code: HCS)

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.

K981805POS T-7000Pos Technologies, Inc.K974208TYTRON C-3000Titronics Research & Development Co.K950986NEUROREADERArtronicsK894772THERMALGRAPHIC ANALYSERMedtech InstrumentsK831995TRENDO-SCOPEGabriel Ent.K822795GABRIEL DIGITRENDGabriel Ent.

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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