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FDA 510(k)

BLOOD GAS SOLUTIONS & CO-OXIMETER SOLU-

K-Number: K830843 · 1983-04-28

Decision Date1983-04-28
Product CodeJKT
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

BLOOD GAS SOLUTIONS & CO-OXIMETER SOLU- is the device name listed in this FDA 510(k) record. The listed applicant is Rna Medical Corp.. It received FDA 510(k) clearance on 1983-04-28 under 510(k) number K830843. The device is classified under product code JKT. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD GAS SOLUTIONS & CO-OXIMETER SOLU-?

BLOOD GAS SOLUTIONS & CO-OXIMETER SOLU- is a medical device that received FDA 510(k) clearance on 1983-04-28. The listed applicant is Rna Medical Corp.. The 510(k) number is K830843.

When did BLOOD GAS SOLUTIONS & CO-OXIMETER SOLU- receive FDA 510(k) clearance?

BLOOD GAS SOLUTIONS & CO-OXIMETER SOLU- received FDA 510(k) clearance on 1983-04-28, under 510(k) number K830843.

Who is the listed applicant for BLOOD GAS SOLUTIONS & CO-OXIMETER SOLU-?

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

What is the FDA product code for BLOOD GAS SOLUTIONS & CO-OXIMETER SOLU-?

The FDA product code for BLOOD GAS SOLUTIONS & CO-OXIMETER SOLU- is JKT.

Related Clinical Trials

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.

Other records listing Rna Medical 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.

Related Devices (Code: JKT)

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.

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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