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FDA 510(k)

YELLOW IRIS URINALYSIS WRKSTA W/IRISCOPE BDY FLU

K-Number: K914256 · 1992-05-01

ApplicantIntl. Remote Imaging Systems
Decision Date1992-05-01
Product CodeGKL
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

YELLOW IRIS URINALYSIS WRKSTA W/IRISCOPE BDY FLU is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Remote Imaging Systems. It received FDA 510(k) clearance on 1992-05-01 under 510(k) number K914256. The device is classified under product code GKL. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YELLOW IRIS URINALYSIS WRKSTA W/IRISCOPE BDY FLU?

YELLOW IRIS URINALYSIS WRKSTA W/IRISCOPE BDY FLU is a medical device that received FDA 510(k) clearance on 1992-05-01. The listed applicant is Intl. Remote Imaging Systems. The 510(k) number is K914256.

When did YELLOW IRIS URINALYSIS WRKSTA W/IRISCOPE BDY FLU receive FDA 510(k) clearance?

YELLOW IRIS URINALYSIS WRKSTA W/IRISCOPE BDY FLU received FDA 510(k) clearance on 1992-05-01, under 510(k) number K914256.

Who is the listed applicant for YELLOW IRIS URINALYSIS WRKSTA W/IRISCOPE BDY FLU?

The FDA 510(k) record lists Intl. Remote Imaging Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YELLOW IRIS URINALYSIS WRKSTA W/IRISCOPE BDY FLU?

The FDA product code for YELLOW IRIS URINALYSIS WRKSTA W/IRISCOPE BDY FLU is GKL.

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Other records listing Intl. Remote Imaging Systems 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.

K022774IQ 200 SYSTEMK000373939UDX URINE PATHOLOGY SYSTEMK972141THE YELLOW IRIS URINALYSIS WORKSTATIONK953116WHITE IRIS LEUKOCYTE DIFFERENTIAL ANALYZERK960054900UDX URINE PATHOLOGY SYSTEMK954006YELLOW IRIS URINALYSIS WORKSTATION W/IRISCOPE BODY FLUID ANALYSIS CAPABILITY

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Related Devices (Code: GKL)

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.

K152776Glocyte Automated Cell Counter SystemAdvanced Instruments, Inc.K091539IQ 200 URINE ANALIZER BODY FLUIDS MODULEIris DiagnosticsK071652HEMOCUE WBC SYSTEMHemocue ABK051693MODIFICATION TO BAYER ADVIA 2120 HEMATOLOGY ANALYZER WITH AUTOSLIDE SYSTEMBayer Healthcare, LLCK050235IQ 200 URINE ANALYZER BODY FLUIDS MODULEIris International, Inc.K032677SYSMEX POCH-100ISysmex America, 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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