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FDA 510(k)

MODEL T-1 OXYGEN ANALYZER

K-Number: K863158 · 1986-11-13

ApplicantChrysalis Systems, Inc.
Decision Date1986-11-13
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL T-1 OXYGEN ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Chrysalis Systems, Inc.. It received FDA 510(k) clearance on 1986-11-13 under 510(k) number K863158. 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 MODEL T-1 OXYGEN ANALYZER?

MODEL T-1 OXYGEN ANALYZER is a medical device that received FDA 510(k) clearance on 1986-11-13. The listed applicant is Chrysalis Systems, Inc.. The 510(k) number is K863158.

When did MODEL T-1 OXYGEN ANALYZER receive FDA 510(k) clearance?

MODEL T-1 OXYGEN ANALYZER received FDA 510(k) clearance on 1986-11-13, under 510(k) number K863158.

Who is the listed applicant for MODEL T-1 OXYGEN ANALYZER?

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

What is the FDA product code for MODEL T-1 OXYGEN ANALYZER?

The FDA product code for MODEL T-1 OXYGEN ANALYZER 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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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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