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FDA 510(k)

OXEQUIP MODEL 34 MED*STAR OXYGEN MONITOR

K-Number: K792356 · 1979-12-04

ApplicantOxequip Health Ind.
Decision Date1979-12-04
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXEQUIP MODEL 34 MED*STAR OXYGEN MONITOR 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 1979-12-04 under 510(k) number K792356. 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 OXEQUIP MODEL 34 MED*STAR OXYGEN MONITOR?

OXEQUIP MODEL 34 MED*STAR OXYGEN MONITOR is a medical device that received FDA 510(k) clearance on 1979-12-04. The listed applicant is Oxequip Health Ind.. The 510(k) number is K792356.

When did OXEQUIP MODEL 34 MED*STAR OXYGEN MONITOR receive FDA 510(k) clearance?

OXEQUIP MODEL 34 MED*STAR OXYGEN MONITOR received FDA 510(k) clearance on 1979-12-04, under 510(k) number K792356.

Who is the listed applicant for OXEQUIP MODEL 34 MED*STAR OXYGEN MONITOR?

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 OXEQUIP MODEL 34 MED*STAR OXYGEN MONITOR?

The FDA product code for OXEQUIP MODEL 34 MED*STAR 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 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.

K833496OXYGEN MONITOR/CONTROLLERK812624OXEQUIP CONDUCTIVE & NON ANES. BREATHK811987OXY-QUIK MARK IV OXYGEN INHALATORK800369TRI PAC MOUTH PROP

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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