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FDA 510(k)

TECHNICON FAST-LC SYS. ANTICONVU DRUGS

K-Number: K791979 · 1979-11-13

ApplicantTechnicon Instruments Corp.
Decision Date1979-11-13
Product CodeDPE
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

TECHNICON FAST-LC SYS. ANTICONVU DRUGS is the device name listed in this FDA 510(k) record. The listed applicant is Technicon Instruments Corp.. It received FDA 510(k) clearance on 1979-11-13 under 510(k) number K791979. The device is classified under product code DPE. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNICON FAST-LC SYS. ANTICONVU DRUGS?

TECHNICON FAST-LC SYS. ANTICONVU DRUGS is a medical device that received FDA 510(k) clearance on 1979-11-13. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K791979.

When did TECHNICON FAST-LC SYS. ANTICONVU DRUGS receive FDA 510(k) clearance?

TECHNICON FAST-LC SYS. ANTICONVU DRUGS received FDA 510(k) clearance on 1979-11-13, under 510(k) number K791979.

Who is the listed applicant for TECHNICON FAST-LC SYS. ANTICONVU DRUGS?

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

What is the FDA product code for TECHNICON FAST-LC SYS. ANTICONVU DRUGS?

The FDA product code for TECHNICON FAST-LC SYS. ANTICONVU DRUGS is DPE.

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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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