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FDA 510(k)

CEDIA DAU BARBITURATE ASSAY

K-Number: K936030 · 1994-03-22

ApplicantMicrogenics Corp.
Decision Date1994-03-22
Product CodeDIS
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

CEDIA DAU BARBITURATE ASSAY is the device name listed in this FDA 510(k) record. The listed applicant is Microgenics Corp.. It received FDA 510(k) clearance on 1994-03-22 under 510(k) number K936030. The device is classified under product code DIS. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEDIA DAU BARBITURATE ASSAY?

CEDIA DAU BARBITURATE ASSAY is a medical device that received FDA 510(k) clearance on 1994-03-22. The listed applicant is Microgenics Corp.. The 510(k) number is K936030.

When did CEDIA DAU BARBITURATE ASSAY receive FDA 510(k) clearance?

CEDIA DAU BARBITURATE ASSAY received FDA 510(k) clearance on 1994-03-22, under 510(k) number K936030.

Who is the listed applicant for CEDIA DAU BARBITURATE ASSAY?

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

What is the FDA product code for CEDIA DAU BARBITURATE ASSAY?

The FDA product code for CEDIA DAU BARBITURATE ASSAY is DIS.

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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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