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FDA 510(k)

MASTERSCREEN & OXYCON CPX

K-Number: K072323 · 2007-10-10

ApplicantViasys Healthcare GmbH
Decision Date2007-10-10
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MASTERSCREEN & OXYCON CPX is the device name listed in this FDA 510(k) record. The listed applicant is Viasys Healthcare GmbH. It received FDA 510(k) clearance on 2007-10-10 under 510(k) number K072323. The device is classified under product code BZC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASTERSCREEN & OXYCON CPX?

MASTERSCREEN & OXYCON CPX is a medical device that received FDA 510(k) clearance on 2007-10-10. The listed applicant is Viasys Healthcare GmbH. The 510(k) number is K072323.

When did MASTERSCREEN & OXYCON CPX receive FDA 510(k) clearance?

MASTERSCREEN & OXYCON CPX received FDA 510(k) clearance on 2007-10-10, under 510(k) number K072323.

Who is the listed applicant for MASTERSCREEN & OXYCON CPX?

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

What is the FDA product code for MASTERSCREEN & OXYCON CPX?

The FDA product code for MASTERSCREEN & OXYCON CPX is BZC.

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Other records listing Viasys Healthcare GmbH 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.

K092324SPIROPROK091412CLEAN PEAK FLOW METERK091505COR12+K081823MASTERSCREEN PAED - BABY BODYK080510VIP PULMONARY FUNCTION SYSTEMK080734FLOWSCREEN, FLOWSCREEN/CORSCREEN, FLOWSCREEN CT

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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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