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FDA 510(k)

OXYGEN ANALYZER MODEL 800 SERIES

K-Number: K873068 · 1987-10-20

ApplicantSalter Instrumentation, Inc.
Decision Date1987-10-20
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXYGEN ANALYZER MODEL 800 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Salter Instrumentation, Inc.. It received FDA 510(k) clearance on 1987-10-20 under 510(k) number K873068. 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 ANALYZER MODEL 800 SERIES?

OXYGEN ANALYZER MODEL 800 SERIES is a medical device that received FDA 510(k) clearance on 1987-10-20. The listed applicant is Salter Instrumentation, Inc.. The 510(k) number is K873068.

When did OXYGEN ANALYZER MODEL 800 SERIES receive FDA 510(k) clearance?

OXYGEN ANALYZER MODEL 800 SERIES received FDA 510(k) clearance on 1987-10-20, under 510(k) number K873068.

Who is the listed applicant for OXYGEN ANALYZER MODEL 800 SERIES?

The FDA 510(k) record lists Salter Instrumentation, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OXYGEN ANALYZER MODEL 800 SERIES?

The FDA product code for OXYGEN ANALYZER MODEL 800 SERIES is CCL.

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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

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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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