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FDA 510(k)

URINE CALIBRATORS AND CONTROLS MODIFICATION

K-Number: K935101 · 1994-01-27

ApplicantDiagnostic Reagents, Inc.
Decision Date1994-01-27
Product CodeDKB
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

URINE CALIBRATORS AND CONTROLS MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Reagents, Inc.. It received FDA 510(k) clearance on 1994-01-27 under 510(k) number K935101. The device is classified under product code DKB. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URINE CALIBRATORS AND CONTROLS MODIFICATION?

URINE CALIBRATORS AND CONTROLS MODIFICATION is a medical device that received FDA 510(k) clearance on 1994-01-27. The listed applicant is Diagnostic Reagents, Inc.. The 510(k) number is K935101.

When did URINE CALIBRATORS AND CONTROLS MODIFICATION receive FDA 510(k) clearance?

URINE CALIBRATORS AND CONTROLS MODIFICATION received FDA 510(k) clearance on 1994-01-27, under 510(k) number K935101.

Who is the listed applicant for URINE CALIBRATORS AND CONTROLS MODIFICATION?

The FDA 510(k) record lists Diagnostic Reagents, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for URINE CALIBRATORS AND CONTROLS MODIFICATION?

The FDA product code for URINE CALIBRATORS AND CONTROLS MODIFICATION is DKB.

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Other records listing Diagnostic Reagents, Inc. 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.

K983268MODIFICATION OF TRICYCLIC SERUM TOX EIA ASSAYK983812NAPA EIA ASSAYK983323DIGOXIN IMMUNOASSAYK983280VANCOMYCIN EIA ASSAYK983159DRUGS OF ABUSE URINE CALIBRATORS AND CONTROLSK973102LIDOCAINE EIA ASSAY

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Related Devices (Code: DKB)

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.

K120936ABBOTT TDM MULTICONSTITUENT CALIBRATOR, THERMO SCIENTIFIC QMS MULTI-CONSTITUENT CALIBRATORSMicrogenics CorporationK092266RANDOX METHAMPHETAMINE ASSAYRandox Laboratories, Ltd.K101752THERMO SCIENTIFIC CEDIA MULTI-DRUG OFT CALIBRATORSMicrogenics Corp.K090939ROCHE C.F.A.S. DAT QUALITATIVE PLUS CLINICAL CALIBRATOR AND CONTROL SET DAT CLINICAL, MODELS 04590856 190, 04500873 190Roche DiagnosticsK090900ADVIA CHEMISTRY DRUG CALIBRATOR II, MODEL 10376771Siemens Healthcare DiagnosticsK062162DIMENSION VISTA SYSTEM DRUGS OF ABUSE CALIBRATOR (UDAT CAL - KC510)Dade Behring, Inc.

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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