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FDA 510(k)

TT AND HNTT BY HEMOCHRON

K-Number: K900126 · 1990-02-05

ApplicantInternational Technidyne Corp.
Decision Date1990-02-05
Product CodeGJA
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

TT AND HNTT BY HEMOCHRON is the device name listed in this FDA 510(k) record. The listed applicant is International Technidyne Corp.. It received FDA 510(k) clearance on 1990-02-05 under 510(k) number K900126. The device is classified under product code GJA. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TT AND HNTT BY HEMOCHRON?

TT AND HNTT BY HEMOCHRON is a medical device that received FDA 510(k) clearance on 1990-02-05. The listed applicant is International Technidyne Corp.. The 510(k) number is K900126.

When did TT AND HNTT BY HEMOCHRON receive FDA 510(k) clearance?

TT AND HNTT BY HEMOCHRON received FDA 510(k) clearance on 1990-02-05, under 510(k) number K900126.

Who is the listed applicant for TT AND HNTT BY HEMOCHRON?

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

What is the FDA product code for TT AND HNTT BY HEMOCHRON?

The FDA product code for TT AND HNTT BY HEMOCHRON is GJA.

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Related Devices (Code: GJA)

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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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