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FDA 510(k)

MT II SYSTEM - SERUM ALBUMIN

K-Number: K761329 · 1977-03-21

ApplicantTechnicon Instruments Corp.
Decision Date1977-03-21
Product CodeCIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MT II SYSTEM - SERUM ALBUMIN 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 1977-03-21 under 510(k) number K761329. The device is classified under product code CIX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MT II SYSTEM - SERUM ALBUMIN?

MT II SYSTEM - SERUM ALBUMIN is a medical device that received FDA 510(k) clearance on 1977-03-21. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K761329.

When did MT II SYSTEM - SERUM ALBUMIN receive FDA 510(k) clearance?

MT II SYSTEM - SERUM ALBUMIN received FDA 510(k) clearance on 1977-03-21, under 510(k) number K761329.

Who is the listed applicant for MT II SYSTEM - SERUM ALBUMIN?

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 SYSTEM - SERUM ALBUMIN?

The FDA product code for MT II SYSTEM - SERUM ALBUMIN is CIX.

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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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