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FDA 510(k)

COBE CMS-FS MEMBRANE OXYGENATOR

K-Number: K926467 · 1993-11-09

ApplicantCobe Cardiovascular, Inc.
Decision Date1993-11-09
Product CodeDTZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

COBE CMS-FS MEMBRANE OXYGENATOR is the device name listed in this FDA 510(k) record. The listed applicant is Cobe Cardiovascular, Inc.. It received FDA 510(k) clearance on 1993-11-09 under 510(k) number K926467. The device is classified under product code DTZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COBE CMS-FS MEMBRANE OXYGENATOR?

COBE CMS-FS MEMBRANE OXYGENATOR is a medical device that received FDA 510(k) clearance on 1993-11-09. The listed applicant is Cobe Cardiovascular, Inc.. The 510(k) number is K926467.

When did COBE CMS-FS MEMBRANE OXYGENATOR receive FDA 510(k) clearance?

COBE CMS-FS MEMBRANE OXYGENATOR received FDA 510(k) clearance on 1993-11-09, under 510(k) number K926467.

Who is the listed applicant for COBE CMS-FS MEMBRANE OXYGENATOR?

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

What is the FDA product code for COBE CMS-FS MEMBRANE OXYGENATOR?

The FDA product code for COBE CMS-FS MEMBRANE OXYGENATOR is DTZ.

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Other records listing Cobe Cardiovascular, Inc. 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.

K050111SMARXT BMR 1900 CLOSED VENOUS RESERVOIR BAGK042473COBE ANGEL WHOLE BLOOD SEPARATION SYSTEMK040184DIDECO MICRO 40 PH.I.S.I.O. ADULT ARTERIAL FILTERK033641SMARXT VVR4000I PLUS FILTERED HARDSHELL VENOUS RESERVOIR, MODEL 439914800K030462COBE REVOLUTION CENTRIFUGAL BLOOD PUMP WITH PC, MODEL 050300700K021830SORIN BIOMEDICA SMARXT BCD VANGUARD SURFACE MODIFIED CARDIOPLEGIA SYSTEM

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Related Devices (Code: DTZ)

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.

K261438HORIZON 8AF (Integrated OXY MODULE 8AF and Horizon CVR) (US5305)Eurosets S.R.LK253838Lifemotion Disposable Membrane OxygenatorLifemotion Medical Technology Co., Ltd.K240934Quantum Perfusion Blood Oxygenator ECC VT160-E3 (VT160-E3); Quantum Perfusion Blood Oxygenator ECC VT200-E3 (VT200-E3); Quantum Perfusion Blood Oxygenator VT75- E3 (VT75- E3);Spectrum Medical S.R.L.K250821Horizon AF Plus System (Integrated A.L. One AF Plus OXYGENATOR and Horizon CVR) (US5300); A.L. One AF Plus OXYGENATOR (US5204); Horizon CVR (US5073)Eurosets S.R.LK242503Trilly Pediatric Oxygenator with Integrated Arterial Filter (US5232)Eurosets S.R.LK231982Quantum Perfusion Blood Oxygenator VT75-E1, Quantum Perfusion Blood Oxygenator VT75-E2Qura S.R.L

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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