Blood And Plasma Warming Devices

Device, Warming. Blood And Plasma

Device Classification Under Section 513(f)(2)(de Novo) // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration   Follow FDA En Español Search FDA   Home Fo

The following data is part of a De Novo classification by Device Classification Under Section 513(f)(2)(de Novo) // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.s. Food & Drug Administration   Follow Fda En Español Search Fda   Home Fo with the FDA for Blood And Plasma Warming Devices.

Pre-market Notification Details

DeNovo IDDK812311
Device Name:Blood And Plasma Warming Devices
ClassificationDevice, Warming. Blood And Plasma
Applicant
ContactDevice Classification Under Section 513(f)(2)(de N
Product CodeKZL  
CFR Regulation Number864.9205 [🔎]
DecisionSubstantially Equivalent (SE)
510(k) Premarket NotificationDevice Classification Under Section 513(f)(2)(de Novo) // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Lin
Review Advisory BoardHematology
Classification AdvisoryHematology
Type510(k) Traditional
Date Received1981-08-17
Decision Date1981-09-16
Reclassification Order:Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases

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