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FDA 510(k)

CLINICAL BLOOD GAS MIXTURES

K-Number: K964475 · 1996-12-06

ApplicantOxarc, Inc.
Decision Date1996-12-06
Product CodeJIS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CLINICAL BLOOD GAS MIXTURES is the device name listed in this FDA 510(k) record. The listed applicant is Oxarc, Inc.. It received FDA 510(k) clearance on 1996-12-06 under 510(k) number K964475. 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 CLINICAL BLOOD GAS MIXTURES?

CLINICAL BLOOD GAS MIXTURES is a medical device that received FDA 510(k) clearance on 1996-12-06. The listed applicant is Oxarc, Inc.. The 510(k) number is K964475.

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

CLINICAL BLOOD GAS MIXTURES received FDA 510(k) clearance on 1996-12-06, under 510(k) number K964475.

Who is the listed applicant for CLINICAL BLOOD GAS MIXTURES?

The FDA 510(k) record lists Oxarc, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLINICAL BLOOD GAS MIXTURES?

The FDA product code for CLINICAL BLOOD GAS MIXTURES is JIS.

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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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