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FDA 510(k)

CYBERLAB HIGH VOLUME DRUG TESTING SYSTEM

K-Number: K892060 · 1989-08-10

ApplicantSyva Co.
Decision Date1989-08-10
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CYBERLAB HIGH VOLUME DRUG TESTING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Syva Co.. It received FDA 510(k) clearance on 1989-08-10 under 510(k) number K892060. 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 CYBERLAB HIGH VOLUME DRUG TESTING SYSTEM?

CYBERLAB HIGH VOLUME DRUG TESTING SYSTEM is a medical device that received FDA 510(k) clearance on 1989-08-10. The listed applicant is Syva Co.. The 510(k) number is K892060.

When did CYBERLAB HIGH VOLUME DRUG TESTING SYSTEM receive FDA 510(k) clearance?

CYBERLAB HIGH VOLUME DRUG TESTING SYSTEM received FDA 510(k) clearance on 1989-08-10, under 510(k) number K892060.

Who is the listed applicant for CYBERLAB HIGH VOLUME DRUG TESTING SYSTEM?

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 CYBERLAB HIGH VOLUME DRUG TESTING SYSTEM?

The FDA product code for CYBERLAB HIGH VOLUME DRUG TESTING SYSTEM is JQP.

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Other records listing Syva Co. as applicant

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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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