FDA 510(k)

COBE HVR 2200 HARDSHELL VENOUS RESERVOIR, FILTERED

K-Number: K994389 · 2000-03-27

Decision Date2000-03-27

Product CodeDTN

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

COBE HVR 2200 HARDSHELL VENOUS RESERVOIR, FILTERED 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 2000-03-27 under 510(k) number K994389. 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 COBE HVR 2200 HARDSHELL VENOUS RESERVOIR, FILTERED?

COBE HVR 2200 HARDSHELL VENOUS RESERVOIR, FILTERED is a medical device that received FDA 510(k) clearance on 2000-03-27. The listed applicant is Cobe Cardiovascular, Inc.. The 510(k) number is K994389.

When did COBE HVR 2200 HARDSHELL VENOUS RESERVOIR, FILTERED receive FDA 510(k) clearance?

COBE HVR 2200 HARDSHELL VENOUS RESERVOIR, FILTERED received FDA 510(k) clearance on 2000-03-27, under 510(k) number K994389.

Who is the listed applicant for COBE HVR 2200 HARDSHELL VENOUS RESERVOIR, FILTERED?

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 HVR 2200 HARDSHELL VENOUS RESERVOIR, FILTERED?

The FDA product code for COBE HVR 2200 HARDSHELL VENOUS RESERVOIR, FILTERED is DTN.

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Other records listing Cobe Cardiovascular, Inc. as applicant

K050111SMARXT BMR 1900 CLOSED VENOUS RESERVOIR BAG K042473COBE ANGEL WHOLE BLOOD SEPARATION SYSTEM K040184DIDECO MICRO 40 PH.I.S.I.O. ADULT ARTERIAL FILTER K033641SMARXT VVR4000I PLUS FILTERED HARDSHELL VENOUS RESERVOIR, MODEL 439914800 K030462COBE REVOLUTION CENTRIFUGAL BLOOD PUMP WITH PC, MODEL 050300700 K021830SORIN BIOMEDICA SMARXT BCD VANGUARD SURFACE MODIFIED CARDIOPLEGIA SYSTEM

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Related Devices (Code: DTN)

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 Surgery K223361BMR 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.