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FDA 510(k)

BLOOD GAS FLUSH SOL. & FLUSH AGENT 1302

K-Number: K842519 · 1984-08-17

ApplicantRna Medical Corp.
Decision Date1984-08-17
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BLOOD GAS FLUSH SOL. & FLUSH AGENT 1302 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 1984-08-17 under 510(k) number K842519. The device is classified under product code CHL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD GAS FLUSH SOL. & FLUSH AGENT 1302?

BLOOD GAS FLUSH SOL. & FLUSH AGENT 1302 is a medical device that received FDA 510(k) clearance on 1984-08-17. The listed applicant is Rna Medical Corp.. The 510(k) number is K842519.

When did BLOOD GAS FLUSH SOL. & FLUSH AGENT 1302 receive FDA 510(k) clearance?

BLOOD GAS FLUSH SOL. & FLUSH AGENT 1302 received FDA 510(k) clearance on 1984-08-17, under 510(k) number K842519.

Who is the listed applicant for BLOOD GAS FLUSH SOL. & FLUSH AGENT 1302?

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 FLUSH SOL. & FLUSH AGENT 1302?

The FDA product code for BLOOD GAS FLUSH SOL. & FLUSH AGENT 1302 is CHL.

Related Clinical Trials

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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.

K851362STANDARD SOLUTION OF CONDUCTIVITY & MEASUREMENT OFK844589OSMOLARITY STANDARDSK842131FORMACLEAR- & MULTIPLEK830843BLOOD GAS SOLUTIONS & CO-OXIMETER SOLU-K813447SOLUTIONS & BUFFERS FOR BLOOD GAS INSTR

Related Devices (Code: CHL)

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.

K252207ABL90 FLEX PLUS System, safeCLINITUBESRadiometer Medicals ApsK244014i-STAT CG4+ cartridge with the i-STAT 1 SystemAbbott Point of Care, Inc.K240998ABL90 FLEX PLUS SystemRadiometer Medicals ApsK230285i-STAT CG8+ cartridge with the i-STAT 1 SystemAbbott Point of Care, Inc.K221900Stat Profile Prime Plus Analyzer SystemNova Biomedical CorporationK223857i-STAT G3+ cartridge with the i-STAT 1 SystemAbbott Point of Care, 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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