Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MPS 3 ND Myocardial Protection System

K-Number: K201984 · 2020-11-20

ApplicantQuest Medical, Inc.
Decision Date2020-11-20
Product CodeDTR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MPS 3 ND Myocardial Protection System is the device name listed in this FDA 510(k) record. The listed applicant is Quest Medical, Inc.. It received FDA 510(k) clearance on 2020-11-20 under 510(k) number K201984. 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 MPS 3 ND Myocardial Protection System?

MPS 3 ND Myocardial Protection System is a medical device that received FDA 510(k) clearance on 2020-11-20. The listed applicant is Quest Medical, Inc.. The 510(k) number is K201984.

When did MPS 3 ND Myocardial Protection System receive FDA 510(k) clearance?

MPS 3 ND Myocardial Protection System received FDA 510(k) clearance on 2020-11-20, under 510(k) number K201984.

Who is the listed applicant for MPS 3 ND Myocardial Protection System?

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

What is the FDA product code for MPS 3 ND Myocardial Protection System?

The FDA product code for MPS 3 ND Myocardial Protection System is DTR.

Other records listing Quest Medical, 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.

K241058Lyka® PORT Needle Free Access Device (4170Y)K213846Q2 Blood Administration SetsK213588Q2 IV Administration SetsK202672Precision Delivery Infusion SetK200438MPS 3 Myocardial Protection SystemK182442MiniGuard Arterial Safety Valve

View all 10 devices →

Related Devices (Code: DTR)

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.

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.

↑