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FDA 510(k)

CIBA CORNING 288 PH/BLOOD GAS SYSTEM

K-Number: K872888 · 1987-08-25

ApplicantCiba Corning Diagnostics Corp.
Decision Date1987-08-25
Product CodeJQY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CIBA CORNING 288 PH/BLOOD GAS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ciba Corning Diagnostics Corp.. It received FDA 510(k) clearance on 1987-08-25 under 510(k) number K872888. The device is classified under product code JQY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIBA CORNING 288 PH/BLOOD GAS SYSTEM?

CIBA CORNING 288 PH/BLOOD GAS SYSTEM is a medical device that received FDA 510(k) clearance on 1987-08-25. The listed applicant is Ciba Corning Diagnostics Corp.. The 510(k) number is K872888.

When did CIBA CORNING 288 PH/BLOOD GAS SYSTEM receive FDA 510(k) clearance?

CIBA CORNING 288 PH/BLOOD GAS SYSTEM received FDA 510(k) clearance on 1987-08-25, under 510(k) number K872888.

Who is the listed applicant for CIBA CORNING 288 PH/BLOOD GAS SYSTEM?

The FDA 510(k) record lists Ciba Corning Diagnostics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CIBA CORNING 288 PH/BLOOD GAS SYSTEM?

The FDA product code for CIBA CORNING 288 PH/BLOOD GAS SYSTEM is JQY.

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Other records listing Ciba Corning Diagnostics Corp. 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.

K962559ACS CORTISOL IMMUNOASSAYK963251CIBA CORNING ACS;180 DPD ASSAYK961807CERTAIN HCT LEVEL A & LEVEL B/CVM HCT LEVELS 1,2,3, & 4K961657CIBA CORNING 400 SYSTEMK962021CIBA CORNING 348 SYSTEMK962126ACS CKMB II IMMUNOASSAY

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Related Devices (Code: JQY)

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.

K952178PH-DETECT TESTDiagnostic Reagents, Inc.K905146OLYMPUS URINE PHDiagnostic SystemsK770347METER, PH, DIGITAL, MODEL 3560Beckman Instruments, Inc.K770352METER, IV PH, MODEL EXPANDOMATICBeckman Instruments, Inc.K770351METER, IV PH, MODEL ZEROMATICBeckman Instruments, Inc.K760789PH METER-130 (.001 PH)Corning Medical & Scientific

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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