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FDA 510(k)

COBE OPTIMIN HOLLOW FIBER MEMBRANE OXYGENATOR

K-Number: K991452 · 1999-10-07

ApplicantCobe Cardiovascular, Inc.
Decision Date1999-10-07
Product CodeDTZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

COBE OPTIMIN HOLLOW FIBER 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 1999-10-07 under 510(k) number K991452. 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 OPTIMIN HOLLOW FIBER MEMBRANE OXYGENATOR?

COBE OPTIMIN HOLLOW FIBER MEMBRANE OXYGENATOR is a medical device that received FDA 510(k) clearance on 1999-10-07. The listed applicant is Cobe Cardiovascular, Inc.. The 510(k) number is K991452.

When did COBE OPTIMIN HOLLOW FIBER MEMBRANE OXYGENATOR receive FDA 510(k) clearance?

COBE OPTIMIN HOLLOW FIBER MEMBRANE OXYGENATOR received FDA 510(k) clearance on 1999-10-07, under 510(k) number K991452.

Who is the listed applicant for COBE OPTIMIN HOLLOW FIBER 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 OPTIMIN HOLLOW FIBER MEMBRANE OXYGENATOR?

The FDA product code for COBE OPTIMIN HOLLOW FIBER MEMBRANE OXYGENATOR is DTZ.

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Other records listing Cobe Cardiovascular, Inc. as applicant

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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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