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 Mixing And Weighing Devices.
DeNovo ID | DK802608 |
Device Name: | Blood Mixing And Weighing Devices |
Classification | Device, Blood Mixing And Blood Weighing |
Applicant | |
Contact | Device Classification Under Section 513(f)(2)(de N |
Product Code | KSQ |
CFR Regulation Number | 864.9195 [🔎] |
Decision | Substantially Equivalent (SE) |
510(k) Premarket Notification | 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 Lin |
Review Advisory Board | Hematology |
Classification Advisory | Hematology |
Type | 510(k) Traditional |
Date Received | 1980-10-21 |
Decision Date | 1980-12-11 |
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 |