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FDA 510(k)

TYTRON C-3000

K-Number: K974208 · 1998-02-03

ApplicantTitronics Research & Development Co.
Decision Date1998-02-03
Product CodeHCS
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TYTRON C-3000 is the device name listed in this FDA 510(k) record. The listed applicant is Titronics Research & Development Co.. It received FDA 510(k) clearance on 1998-02-03 under 510(k) number K974208. 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 TYTRON C-3000?

TYTRON C-3000 is a medical device that received FDA 510(k) clearance on 1998-02-03. The listed applicant is Titronics Research & Development Co.. The 510(k) number is K974208.

When did TYTRON C-3000 receive FDA 510(k) clearance?

TYTRON C-3000 received FDA 510(k) clearance on 1998-02-03, under 510(k) number K974208.

Who is the listed applicant for TYTRON C-3000?

The FDA 510(k) record lists Titronics Research & Development Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TYTRON C-3000?

The FDA product code for TYTRON C-3000 is HCS.

Related Clinical Trials

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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Other records listing Titronics Research & Development Co. 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.

K032471TYTRON C-500IR CLINICAL INFRARED IMAGING SYSTEM

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.K950986NEUROREADERArtronicsK894772THERMALGRAPHIC ANALYSERMedtech InstrumentsK840487T-METERK.J. ElectronicsK831995TRENDO-SCOPEGabriel Ent.K822795GABRIEL DIGITRENDGabriel Ent.

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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