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FDA 510(k)

MODIFIED MP-4 CARDIOPLEGIA DELIVERY SYSTEM W/CONDU

K-Number: K900640 · 1990-04-20

Applicant3M Company
Decision Date1990-04-20
Product CodeDTR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED MP-4 CARDIOPLEGIA DELIVERY SYSTEM W/CONDU is the device name listed in this FDA 510(k) record. The listed applicant is 3M Company. It received FDA 510(k) clearance on 1990-04-20 under 510(k) number K900640. The device is classified under product code DTR. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED MP-4 CARDIOPLEGIA DELIVERY SYSTEM W/CONDU?

MODIFIED MP-4 CARDIOPLEGIA DELIVERY SYSTEM W/CONDU is a medical device that received FDA 510(k) clearance on 1990-04-20. The listed applicant is 3M Company. The 510(k) number is K900640.

When did MODIFIED MP-4 CARDIOPLEGIA DELIVERY SYSTEM W/CONDU receive FDA 510(k) clearance?

MODIFIED MP-4 CARDIOPLEGIA DELIVERY SYSTEM W/CONDU received FDA 510(k) clearance on 1990-04-20, under 510(k) number K900640.

Who is the listed applicant for MODIFIED MP-4 CARDIOPLEGIA DELIVERY SYSTEM W/CONDU?

The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED MP-4 CARDIOPLEGIA DELIVERY SYSTEM W/CONDU?

The FDA product code for MODIFIED MP-4 CARDIOPLEGIA DELIVERY SYSTEM W/CONDU is DTR.

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Related Devices (Code: DTR)

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K252541Quantum PureFlow Standard Heat Exchanger Medium Flow 1/4 WSpectrum Medical S.R.L.K240908Quantum Micro-Cardioplegia Delivery System; Quantum Micro-Cardioplegia Delivery Module (QMCDM)Spectrum Medical , Ltd.K250150VANGUARD Blood cardioplegia Systems (Vanguard 4:1 Blood cardioplegia set); VANGUARD Blood cardioplegia Systems (Vanguard 4:1 Blood cardioplegia set with shunt); VANGUARD Blood cardioplegia Systems (Vanguard 4:1 Blood Cardioplegia Set Mini)Sorin Group Italia S.R.L.K240190MYOtherm XP Cardioplegia Delivery System with Cortiva BioActive Surface, MYOtherm XP Cardioplegia Delivery System UncoatedMedtronicK223879Quantum PureFlow Standard Heat Exchangers (HX11W-S2, HX11W-S1M and HX11W-S2M)Quara S.R.L.K220110Quantum PureFlow Standard Heat Exchanger and Quantum PureFlow Cardioplegia Heat ExchangerQura 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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