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FDA 510(k)

CEDIA DAU THC CALIBRATORS

K-Number: K935795 · 1994-04-06

ApplicantMicrogenics Corp.
Decision Date1994-04-06
Product CodeDLJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

CEDIA DAU THC CALIBRATORS is the device name listed in this FDA 510(k) record. The listed applicant is Microgenics Corp.. It received FDA 510(k) clearance on 1994-04-06 under 510(k) number K935795. The device is classified under product code DLJ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEDIA DAU THC CALIBRATORS?

CEDIA DAU THC CALIBRATORS is a medical device that received FDA 510(k) clearance on 1994-04-06. The listed applicant is Microgenics Corp.. The 510(k) number is K935795.

When did CEDIA DAU THC CALIBRATORS receive FDA 510(k) clearance?

CEDIA DAU THC CALIBRATORS received FDA 510(k) clearance on 1994-04-06, under 510(k) number K935795.

Who is the listed applicant for CEDIA DAU THC CALIBRATORS?

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 THC CALIBRATORS?

The FDA product code for CEDIA DAU THC CALIBRATORS is DLJ.

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Related Devices (Code: DLJ)

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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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