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FDA 510(k)

EMIT D.A.U. MONOCLONAL AMPHETAMINE/METHAMPHETAMINE

K-Number: K884022 · 1988-10-11

ApplicantSyva Co.
Decision Date1988-10-11
Product CodeDKZ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

EMIT D.A.U. MONOCLONAL AMPHETAMINE/METHAMPHETAMINE is the device name listed in this FDA 510(k) record. The listed applicant is Syva Co.. It received FDA 510(k) clearance on 1988-10-11 under 510(k) number K884022. The device is classified under product code DKZ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMIT D.A.U. MONOCLONAL AMPHETAMINE/METHAMPHETAMINE?

EMIT D.A.U. MONOCLONAL AMPHETAMINE/METHAMPHETAMINE is a medical device that received FDA 510(k) clearance on 1988-10-11. The listed applicant is Syva Co.. The 510(k) number is K884022.

When did EMIT D.A.U. MONOCLONAL AMPHETAMINE/METHAMPHETAMINE receive FDA 510(k) clearance?

EMIT D.A.U. MONOCLONAL AMPHETAMINE/METHAMPHETAMINE received FDA 510(k) clearance on 1988-10-11, under 510(k) number K884022.

Who is the listed applicant for EMIT D.A.U. MONOCLONAL AMPHETAMINE/METHAMPHETAMINE?

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

What is the FDA product code for EMIT D.A.U. MONOCLONAL AMPHETAMINE/METHAMPHETAMINE?

The FDA product code for EMIT D.A.U. MONOCLONAL AMPHETAMINE/METHAMPHETAMINE is DKZ.

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Other records listing Syva Co. 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.

K011878EMIT (R) TOX SALICYLIC ASSAY, MODEL 7SO19UL, EMIT (R) TOX SALICYLIC ACID CALIBRATORS, MODEL 7S109ULK012257EMIT II PLUS MONOCLONAL AMPHETAMINE/METHAMPHETAMINE ASSAY MODEL OSR9C229K011947EMIT 2000 VALPROIC ACID ASSAY, MODEL OSR4G229ULK011528EMIT 2000 PHENOBARBITAL ASSAY, MODEL OSR4D229K011347EMIT 2000 PHENYTOIN ASSAY, MODEL 0SR4A229K993980SYVA EMIT II PLUS ETHYL ALCOHOL ASSAY, MODELS 9K309UL/9K409UL

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Related Devices (Code: DKZ)

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.

K240670DRI Ecstasy Plus AssayMicrogenics CorporationK233019AllTest Multi-Drug Rapid Test Cup; AllTest Multi-Drug Rapid Test Panel; AllTest Multi-Drug Rapid Test Cup Rx; AllTest Multi-Drug Rapid Test Panel RxHangzhou AllTest Biotech Co., Ltd.K231137Xenta Drug Screen Cup, Xenta Drug Screen DipcardXenta Biomedical Science Co., Ltd.K200363Quidel Triage® TOX Drug Screen, 94600Quidel Cardiovascular, Inc.K191099Atlas Multi-Drugs Screening Test Cup, Atlas Multi-Drugs Screening Test PanelAtlas MedicalK182719Quidel Triage TOX Drug Screen, 94600; Quidel Triage® MeterProQuidel Cardiovascular, 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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