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FDA 510(k)

VEO MULTIGAS MONITOR FOR POCKET PC

K-Number: K081601 · 2008-09-04

ApplicantPhasein AB
Decision Date2008-09-04
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VEO MULTIGAS MONITOR FOR POCKET PC is the device name listed in this FDA 510(k) record. The listed applicant is Phasein AB. It received FDA 510(k) clearance on 2008-09-04 under 510(k) number K081601. 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 VEO MULTIGAS MONITOR FOR POCKET PC?

VEO MULTIGAS MONITOR FOR POCKET PC is a medical device that received FDA 510(k) clearance on 2008-09-04. The listed applicant is Phasein AB. The 510(k) number is K081601.

When did VEO MULTIGAS MONITOR FOR POCKET PC receive FDA 510(k) clearance?

VEO MULTIGAS MONITOR FOR POCKET PC received FDA 510(k) clearance on 2008-09-04, under 510(k) number K081601.

Who is the listed applicant for VEO MULTIGAS MONITOR FOR POCKET PC?

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

What is the FDA product code for VEO MULTIGAS MONITOR FOR POCKET PC?

The FDA product code for VEO MULTIGAS MONITOR FOR POCKET PC is CCK.

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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Other records listing Phasein AB 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.

K123043IRMA C02 MODEL 200101; IRMA AX 200601K103604ISA CO2, ISA AX+, ISA OR+K072813EMMA ANALYZER (KPA & MMHG); EMMA MONITOR (KPA & MMHG)K063167EMMA ANALYZER (KPA) AND (MMHG); EMMA MONITOR (KPA) AND (MMHG)

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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