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FDA 510(k)

EMIT CLINICAL PROCESSOR #CP-5000

K-Number: K822932 · 1982-11-05

ApplicantSyva Co.
Decision Date1982-11-05
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EMIT CLINICAL PROCESSOR #CP-5000 is the device name listed in this FDA 510(k) record. The listed applicant is Syva Co.. It received FDA 510(k) clearance on 1982-11-05 under 510(k) number K822932. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMIT CLINICAL PROCESSOR #CP-5000?

EMIT CLINICAL PROCESSOR #CP-5000 is a medical device that received FDA 510(k) clearance on 1982-11-05. The listed applicant is Syva Co.. The 510(k) number is K822932.

When did EMIT CLINICAL PROCESSOR #CP-5000 receive FDA 510(k) clearance?

EMIT CLINICAL PROCESSOR #CP-5000 received FDA 510(k) clearance on 1982-11-05, under 510(k) number K822932.

Who is the listed applicant for EMIT CLINICAL PROCESSOR #CP-5000?

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 CLINICAL PROCESSOR #CP-5000?

The FDA product code for EMIT CLINICAL PROCESSOR #CP-5000 is JQP.

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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: JQP)

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.

K113007BIONIME DIABETES MANAGEMENT SYSTEM VI.0Bionime CorporationK983468FASTTAKE ADAPTER, MODEL # P/N 020-072-01Selfcare, Inc.K964460THE ROBOLITEShai Syg Motion and Innovations, Ltd.K953652PRENVAL IBase Ten Systems, Inc.K934111MR7000 WITH TIME MANAGER SOFTWARE (TMS)Dynatech Laboratories, Inc.K923316EXPRESSO CARTRIDGEBio-Rad Laboratories, 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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