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FDA 510(k)

OXYGEN MEDICELS, CITICELS

K-Number: K041773 · 2004-07-15

ApplicantCity Technology Limited
Decision Date2004-07-15
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXYGEN MEDICELS, CITICELS is the device name listed in this FDA 510(k) record. The listed applicant is City Technology Limited. It received FDA 510(k) clearance on 2004-07-15 under 510(k) number K041773. 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 MEDICELS, CITICELS?

OXYGEN MEDICELS, CITICELS is a medical device that received FDA 510(k) clearance on 2004-07-15. The listed applicant is City Technology Limited. The 510(k) number is K041773.

When did OXYGEN MEDICELS, CITICELS receive FDA 510(k) clearance?

OXYGEN MEDICELS, CITICELS received FDA 510(k) clearance on 2004-07-15, under 510(k) number K041773.

Who is the listed applicant for OXYGEN MEDICELS, CITICELS?

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

What is the FDA product code for OXYGEN MEDICELS, CITICELS?

The FDA product code for OXYGEN MEDICELS, CITICELS 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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