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FDA 510(k)

ANALYZER, OXYGEN, MODEL OM-92

K-Number: K771028 · 1977-07-05

ApplicantCavitron Corp.
Decision Date1977-07-05
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANALYZER, OXYGEN, MODEL OM-92 is the device name listed in this FDA 510(k) record. The listed applicant is Cavitron Corp.. It received FDA 510(k) clearance on 1977-07-05 under 510(k) number K771028. 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 ANALYZER, OXYGEN, MODEL OM-92?

ANALYZER, OXYGEN, MODEL OM-92 is a medical device that received FDA 510(k) clearance on 1977-07-05. The listed applicant is Cavitron Corp.. The 510(k) number is K771028.

When did ANALYZER, OXYGEN, MODEL OM-92 receive FDA 510(k) clearance?

ANALYZER, OXYGEN, MODEL OM-92 received FDA 510(k) clearance on 1977-07-05, under 510(k) number K771028.

Who is the listed applicant for ANALYZER, OXYGEN, MODEL OM-92?

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

What is the FDA product code for ANALYZER, OXYGEN, MODEL OM-92?

The FDA product code for ANALYZER, OXYGEN, MODEL OM-92 is CCL.

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Other records listing Cavitron Corp. 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.

K811582THE PLACERK810207MINOR SURGERY LIGHTK802928SPIROMETRIC COMPUTER #SC-10K801623CAVITRON ULTRASONIC SURG. ASPIR. CUSAK801877SLIT LAMP ATTACHMENTK800869MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALA

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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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