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FDA 510(k)

SCIMED ULTROX TRUE MEMBRANE OXYGEN SYST, ULTROX II

K-Number: K894103 · 1989-09-21

ApplicantScimed Life Systems, Inc.
Decision Date1989-09-21
Product CodeDTZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SCIMED ULTROX TRUE MEMBRANE OXYGEN SYST, ULTROX II is the device name listed in this FDA 510(k) record. The listed applicant is Scimed Life Systems, Inc.. It received FDA 510(k) clearance on 1989-09-21 under 510(k) number K894103. 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 SCIMED ULTROX TRUE MEMBRANE OXYGEN SYST, ULTROX II?

SCIMED ULTROX TRUE MEMBRANE OXYGEN SYST, ULTROX II is a medical device that received FDA 510(k) clearance on 1989-09-21. The listed applicant is Scimed Life Systems, Inc.. The 510(k) number is K894103.

When did SCIMED ULTROX TRUE MEMBRANE OXYGEN SYST, ULTROX II receive FDA 510(k) clearance?

SCIMED ULTROX TRUE MEMBRANE OXYGEN SYST, ULTROX II received FDA 510(k) clearance on 1989-09-21, under 510(k) number K894103.

Who is the listed applicant for SCIMED ULTROX TRUE MEMBRANE OXYGEN SYST, ULTROX II?

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

What is the FDA product code for SCIMED ULTROX TRUE MEMBRANE OXYGEN SYST, ULTROX II?

The FDA product code for SCIMED ULTROX TRUE MEMBRANE OXYGEN SYST, ULTROX II is DTZ.

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Other records listing Scimed Life Systems, 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.

K974241SCIMED INFORMER PRESSURE WIRE SYSTEMK981788SCIMED 6 FRENCH WISEGUIDE GUIDE CATHETERK980360SCIMED QUEST FLOPPY AND MODERATE SUPPORT GUIDE WIRESK974559SCIMED 6 FRENCH IMPULSE ANGIOGRAPHIC CATHETERSK974684SCIMED 7 FRENCH WISEGUIDE GUIDE CATHETERK973945LUGE GUIDE WIRE

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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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