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FDA 510(k)

CEDIA(TM) T UPTAKE

K-Number: K872447 · 1987-08-21

ApplicantMicrogenics Corp.
Decision Date1987-08-21
Product CodeKHQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CEDIA(TM) T UPTAKE is the device name listed in this FDA 510(k) record. The listed applicant is Microgenics Corp.. It received FDA 510(k) clearance on 1987-08-21 under 510(k) number K872447. The device is classified under product code KHQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEDIA(TM) T UPTAKE?

CEDIA(TM) T UPTAKE is a medical device that received FDA 510(k) clearance on 1987-08-21. The listed applicant is Microgenics Corp.. The 510(k) number is K872447.

When did CEDIA(TM) T UPTAKE receive FDA 510(k) clearance?

CEDIA(TM) T UPTAKE received FDA 510(k) clearance on 1987-08-21, under 510(k) number K872447.

Who is the listed applicant for CEDIA(TM) T UPTAKE?

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(TM) T UPTAKE?

The FDA product code for CEDIA(TM) T UPTAKE is KHQ.

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Other records listing Microgenics 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.

K122766THERMO SCIENTIFIC QMS EVEROLIMUS ASSAYK123343THERMO SCIENTIFIC QMS TACROLIMUS ASSAY AND CALIBRATORSK123271ABBOTT PHENOBARBITAL ASSAYK110616THERMO SCIENTIFIC MAS OMNI-IMMUNE, MAS OMNI IMMUNE PROK101754THERMO SCIENTIFIC CEDIA OPIATE OFT ASSAYK101746THERMO SCIENTIFIC CEDIA PHENCYCLIDINE (PCP) OFT ASSAY

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Related Devices (Code: KHQ)

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.

K981375ACE T UPTAKE REAGENT TU CALIBRATORSSchiapparelli Biosystems, Inc.K980088T-UPTAKE MICROPLATE EIAMonobindK970539CHIRON DIAGNOSTICS ACS:180TU PChiron Diagnostics Corp.K964308VITROS IMMUNODIAGNOSTICS PRODUCTS T3 UPTAKE REAGENT PACK (GEM.1025) AND T3 UPTAKE CALIBRATORS (GEM.C025)Johnson & Johnson Clinical Diagnostics, Inc.K961488ELECSYS T-UPTAKE ASSAYBoehringer Mannheim Corp.K954807CEDIA T UPTAKE ASSAYBoehringer Mannheim Corp.

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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