The following data is part of a premarket notification filed by Fujifilm Medical Systems, Usa Inc. with the FDA for Aspire Cristalle.
Device ID | K133972 |
510k Number | K133972 |
Device Name: | ASPIRE CRISTALLE |
Classification | Full Field Digital, System, X-ray, Mammographic |
Applicant | FUJIFILM MEDICAL SYSTEMS, USA INC. 419 WEST AVE. Stanford, CT 06902 |
Contact | Peter Altman |
Correspondent | Peter Altman FUJIFILM MEDICAL SYSTEMS, USA INC. 419 WEST AVE. Stanford, CT 06902 |
Product Code | MUE |
CFR Regulation Number | 892.1715 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-12-26 |
Decision Date | 2014-03-25 |
Summary: | summary |