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FDA 510(k)

MT II - TEST FOR CONTINUOUS FLOW ANAL

K-Number: K761165 · 1976-12-13

Decision Date1976-12-13
Product CodeJJC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MT II - TEST FOR CONTINUOUS FLOW ANAL 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 1976-12-13 under 510(k) number K761165. The device is classified under product code JJC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MT II - TEST FOR CONTINUOUS FLOW ANAL?

MT II - TEST FOR CONTINUOUS FLOW ANAL is a medical device that received FDA 510(k) clearance on 1976-12-13. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K761165.

When did MT II - TEST FOR CONTINUOUS FLOW ANAL receive FDA 510(k) clearance?

MT II - TEST FOR CONTINUOUS FLOW ANAL received FDA 510(k) clearance on 1976-12-13, under 510(k) number K761165.

Who is the listed applicant for MT II - TEST FOR CONTINUOUS FLOW ANAL?

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 MT II - TEST FOR CONTINUOUS FLOW ANAL?

The FDA product code for MT II - TEST FOR CONTINUOUS FLOW ANAL is JJC.

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.

Other records listing Technicon Instruments Corp. 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.

View all 157 devices →

Related Devices (Code: JJC)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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