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FDA 510(k)

OHMEDA MODEL 5200 CO2 MONITOR

K-Number: K843599 · 1984-10-04

ApplicantOhmeda Medical
Decision Date1984-10-04
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OHMEDA MODEL 5200 CO2 MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Medical. It received FDA 510(k) clearance on 1984-10-04 under 510(k) number K843599. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHMEDA MODEL 5200 CO2 MONITOR?

OHMEDA MODEL 5200 CO2 MONITOR is a medical device that received FDA 510(k) clearance on 1984-10-04. The listed applicant is Ohmeda Medical. The 510(k) number is K843599.

When did OHMEDA MODEL 5200 CO2 MONITOR receive FDA 510(k) clearance?

OHMEDA MODEL 5200 CO2 MONITOR received FDA 510(k) clearance on 1984-10-04, under 510(k) number K843599.

Who is the listed applicant for OHMEDA MODEL 5200 CO2 MONITOR?

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

What is the FDA product code for OHMEDA MODEL 5200 CO2 MONITOR?

The FDA product code for OHMEDA MODEL 5200 CO2 MONITOR is CCK.

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Other records listing Ohmeda Medical as applicant

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Related Devices (Code: CCK)

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.

K251641GF-310R Multigas Unit (GF-310R)Nihon Kohden CorporationK261633VisuBreathAffirm Medical Technologies II, LLCK253030Capnostream™35 Portable Respiratory Monitor (PM35MN)Covidien, LLCK250148Medical Gas Analyzer (AG200)Prior Care Science Technology, Ltd.K243956TG-980P CO2 Sensor Kit (TG-980P); TG-980P1 CO2 Sensor Kit (TG-980P1)Nihon Kohden CorporationK2512160184 CO2 Sampling line; 0184T CO2 Sampling line; 0139 CO2 Sampling line; 0182 CO2 Sampling lineBarbaras Development, 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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