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FDA 510(k)

OXYGEN MONITOR/CONTROLLER

K-Number: K833496 · 1983-12-16

ApplicantOxequip Health Ind.
Decision Date1983-12-16
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXYGEN MONITOR/CONTROLLER is the device name listed in this FDA 510(k) record. The listed applicant is Oxequip Health Ind.. It received FDA 510(k) clearance on 1983-12-16 under 510(k) number K833496. 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 OXYGEN MONITOR/CONTROLLER?

OXYGEN MONITOR/CONTROLLER is a medical device that received FDA 510(k) clearance on 1983-12-16. The listed applicant is Oxequip Health Ind.. The 510(k) number is K833496.

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

OXYGEN MONITOR/CONTROLLER received FDA 510(k) clearance on 1983-12-16, under 510(k) number K833496.

Who is the listed applicant for OXYGEN MONITOR/CONTROLLER?

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

What is the FDA product code for OXYGEN MONITOR/CONTROLLER?

The FDA product code for OXYGEN MONITOR/CONTROLLER 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 Oxequip Health Ind. 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.

K812624OXEQUIP CONDUCTIVE & NON ANES. BREATHK811987OXY-QUIK MARK IV OXYGEN INHALATORK800369TRI PAC MOUTH PROPK792356OXEQUIP MODEL 34 MED*STAR OXYGEN MONITOR

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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