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FDA 510(k)

RX300 OXYGEN ANALYZER

K-Number: K024228 · 2003-07-17

ApplicantTeledyne Analytical Instruments
Decision Date2003-07-17
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RX300 OXYGEN ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Teledyne Analytical Instruments. It received FDA 510(k) clearance on 2003-07-17 under 510(k) number K024228. The device is classified under product code CCL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RX300 OXYGEN ANALYZER?

RX300 OXYGEN ANALYZER is a medical device that received FDA 510(k) clearance on 2003-07-17. The listed applicant is Teledyne Analytical Instruments. The 510(k) number is K024228.

When did RX300 OXYGEN ANALYZER receive FDA 510(k) clearance?

RX300 OXYGEN ANALYZER received FDA 510(k) clearance on 2003-07-17, under 510(k) number K024228.

Who is the listed applicant for RX300 OXYGEN ANALYZER?

The FDA 510(k) record lists Teledyne Analytical Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RX300 OXYGEN ANALYZER?

The FDA product code for RX300 OXYGEN ANALYZER is CCL.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Teledyne Analytical Instruments 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.

K024155MX 300 OXYGEN MONITORK001095OXYGEN SENSORS, MODELS CIR, C2R, R13, R15, RI7MED, R22MED, R23, R24MED, R29MED, T1, T2,T4, T7 & UFO130

Related Devices (Code: CCL)

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.

K261389PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1)Salter LabsK251245OxyMinder Pro (10310)Bio-Med Device, Inc.K250002Smart Check O2 (MA0236)Life Spark Medical, LLCK221734Maxtec MaxO2 ME+pMaxtec, LLCK213933Percent Oxygen SensorsCareox, LLCK213948OxyMinderBio-Med Devices, 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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