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FDA 510(k)

SORIN MONOLYTH VENOUS RESERVOIR

K-Number: K933481 · 1993-11-02

ApplicantSorin Biomedical, Inc.
Decision Date1993-11-02
Product CodeDTN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SORIN MONOLYTH VENOUS RESERVOIR is the device name listed in this FDA 510(k) record. The listed applicant is Sorin Biomedical, Inc.. It received FDA 510(k) clearance on 1993-11-02 under 510(k) number K933481. The device is classified under product code DTN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SORIN MONOLYTH VENOUS RESERVOIR?

SORIN MONOLYTH VENOUS RESERVOIR is a medical device that received FDA 510(k) clearance on 1993-11-02. The listed applicant is Sorin Biomedical, Inc.. The 510(k) number is K933481.

When did SORIN MONOLYTH VENOUS RESERVOIR receive FDA 510(k) clearance?

SORIN MONOLYTH VENOUS RESERVOIR received FDA 510(k) clearance on 1993-11-02, under 510(k) number K933481.

Who is the listed applicant for SORIN MONOLYTH VENOUS RESERVOIR?

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

What is the FDA product code for SORIN MONOLYTH VENOUS RESERVOIR?

The FDA product code for SORIN MONOLYTH VENOUS RESERVOIR is DTN.

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Other records listing Sorin Biomedical, 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.

K990103MONOLYTH C 600 AND 1200 HOLLOW FIBER MEMBRANE LUNG WITH INTEGRATED SOFTSHELL VENOUS RESERVOIR , CVR 600 AND 1200 SOFTSHEK963758CODE 150 BLOOD COMPONENT COLLECTION SET AND WITH DIRECT DRAW LINEK963759DIDECO COMPACT-A AND COMPACT-M AUTOTRANSFUSION SYSTEMSK964908VRF40 VENOUS RESERVOIR WITH INTEGRAL CARDIOTOMY FILTERK964907VENOMIDICARD PEDIATRIC VENOUS RESERVOIR WITH INTEGRALCARDIOTOMY FILTER/MIDICARD PEDIATRIC CARDIOTOMY RESERVOIR WITH FILTK961869DIDECO NEWBORN/INFANT ARTERIAL FILTERS: D735 MICRO 20 AND D736 MICRO 40

View all 15 devices →

Related Devices (Code: DTN)

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.

K251783Inspire HCR and HCR DUAL cardiotomy reservoirsSorin Group Italia S.R.L.K241206Quantum Perfusion Hybrid SystemSpectrum Medical S.R.L.K241053MVR™ Venous Reservoir Bag 800 mL; MVR™ Venous Reservoir Bag 1600 mL; MVR™ Venous Reservoir Bag with Cortiva™ BioActive Surface 800 mL; MVR™ Venous Reservoir Bag with Cortiva™ BioActive Surface 1600 mLMedtronic Cardiac SurgeryK223361BMR 1900 PHISIOSorin Group Italia S.R.L.K170583Intersept Filtered Cardiotomy Reservoir with Cortiva BioActive SurfaceMedtronic, Inc.K161733INSPIRE SVR 1200, INSPIRE 6F C, INSPIRE 8F CSorin Group Italia 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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