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FDA 510(k)

LILLIPUT 2 INFANT HOLLOW FIBER OXYGENATOR

K-Number: K971877 · 1997-10-08

ApplicantDideco S.P.A.
Decision Date1997-10-08
Product CodeDTZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LILLIPUT 2 INFANT HOLLOW FIBER OXYGENATOR is the device name listed in this FDA 510(k) record. The listed applicant is Dideco S.P.A.. It received FDA 510(k) clearance on 1997-10-08 under 510(k) number K971877. 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 LILLIPUT 2 INFANT HOLLOW FIBER OXYGENATOR?

LILLIPUT 2 INFANT HOLLOW FIBER OXYGENATOR is a medical device that received FDA 510(k) clearance on 1997-10-08. The listed applicant is Dideco S.P.A.. The 510(k) number is K971877.

When did LILLIPUT 2 INFANT HOLLOW FIBER OXYGENATOR receive FDA 510(k) clearance?

LILLIPUT 2 INFANT HOLLOW FIBER OXYGENATOR received FDA 510(k) clearance on 1997-10-08, under 510(k) number K971877.

Who is the listed applicant for LILLIPUT 2 INFANT HOLLOW FIBER OXYGENATOR?

The FDA 510(k) record lists Dideco S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LILLIPUT 2 INFANT HOLLOW FIBER OXYGENATOR?

The FDA product code for LILLIPUT 2 INFANT HOLLOW FIBER OXYGENATOR is DTZ.

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Other records listing Dideco S.P.A. 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.

K041061D731 MICRO 20 AND D733 MICRO 40 PEDIATRIC ARTERIAL FILTERSK033323D 903 AVANT ADULT HOLLOW FIBER OXYGENATOR AND D 903 AVANT 2 PH.I.S.I.O. ADULT HOLLOW FIBER OXYGENATOR WITH COATINGK033987D735 MICRO 20 AND D736 MICRO 40 NEWBORN-INFANT ARTERIAL FILTERSK033714MVR 1200 PC: SORIN MONOLYTH VENOUS RESERVOIR 1200 PC WITH PHOSPHORYLCHOLINE COATINGK032040IDEAL MIMESYS SYSTEM WITH INTEGRATED VENOUS AIR REMOVAL, CENTRIFUGAL BLOOD PUMP, PUMP BRACKET, ADULT MEMBRANE OXYGENATORK031223SYNTHESIS MIMESYS ADULT MEMBRANE OXYGENATOR

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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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