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FDA 510(k)

MX 300 OXYGEN MONITOR

K-Number: K024155 · 2003-07-17

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

Device Summary

MX 300 OXYGEN MONITOR 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 K024155. 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 MX 300 OXYGEN MONITOR?

MX 300 OXYGEN MONITOR 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 K024155.

When did MX 300 OXYGEN MONITOR receive FDA 510(k) clearance?

MX 300 OXYGEN MONITOR received FDA 510(k) clearance on 2003-07-17, under 510(k) number K024155.

Who is the listed applicant for MX 300 OXYGEN MONITOR?

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 MX 300 OXYGEN MONITOR?

The FDA product code for MX 300 OXYGEN MONITOR 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.

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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.

K024228RX300 OXYGEN ANALYZERK001095OXYGEN 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

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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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