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FDA 510(k)

BLOOD GAS MIXTURE

K-Number: K954546 · 1995-12-28

ApplicantLiquid Technology Corp.
Decision Date1995-12-28
Product CodeJIS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BLOOD GAS MIXTURE is the device name listed in this FDA 510(k) record. The listed applicant is Liquid Technology Corp.. It received FDA 510(k) clearance on 1995-12-28 under 510(k) number K954546. The device is classified under product code JIS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD GAS MIXTURE?

BLOOD GAS MIXTURE is a medical device that received FDA 510(k) clearance on 1995-12-28. The listed applicant is Liquid Technology Corp.. The 510(k) number is K954546.

When did BLOOD GAS MIXTURE receive FDA 510(k) clearance?

BLOOD GAS MIXTURE received FDA 510(k) clearance on 1995-12-28, under 510(k) number K954546.

Who is the listed applicant for BLOOD GAS MIXTURE?

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

What is the FDA product code for BLOOD GAS MIXTURE?

The FDA product code for BLOOD GAS MIXTURE is JIS.

Related Clinical Trials

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Other records listing Liquid Technology 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.

K954542LUNG DIFFUSION MIXTUREK954544LASER GAS MIXTURE

Related Devices (Code: JIS)

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.

K122126DIRECT LDL/HDL CHOLESTEROL CALIBRATORRandox Laboratories LimitedK061251DIMENSION VISTA TOTAL IRON BINDING CAPACITY CALIBRATORDade Behring, Inc.K060266DIMENSION IRON CALIBRATORDade Behring, Inc.K053104DIMENSION CARDIOPHASE HIGH SENSITIVITY C-REACTIVE PROTEIN CALIBRATORDade Behring, Inc.K032697DIMENSION TOTAL TRIIODOTHYRONINE CALIBRATOR (RC414)Dade Behring, Inc.K032608GONOTEC CALIBRATION SOLUTION 300 MOSMOL/KG FOR OSMOMETERGonotec Gesellschaft Fuer Mess-Und Regeltechnik MB

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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