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FDA 510(k)

DMA OXYGEN MONITOR

K-Number: K852823 · 1985-10-29

ApplicantFerguson Medical
Decision Date1985-10-29
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DMA OXYGEN MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Ferguson Medical. It received FDA 510(k) clearance on 1985-10-29 under 510(k) number K852823. 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 DMA OXYGEN MONITOR?

DMA OXYGEN MONITOR is a medical device that received FDA 510(k) clearance on 1985-10-29. The listed applicant is Ferguson Medical. The 510(k) number is K852823.

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

DMA OXYGEN MONITOR received FDA 510(k) clearance on 1985-10-29, under 510(k) number K852823.

Who is the listed applicant for DMA OXYGEN MONITOR?

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

What is the FDA product code for DMA OXYGEN MONITOR?

The FDA product code for DMA OXYGEN MONITOR is CCL.

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Other records listing Ferguson Medical as applicant

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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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