The following data is part of a premarket notification filed by Ge Medical Systems Scs with the FDA for Gsi Viewer With Gsi Fat Option.
Device ID | K180225 |
510k Number | K180225 |
Device Name: | GSI Viewer With GSI Fat Option |
Classification | System, X-ray, Tomography, Computed |
Applicant | GE Medical Systems SCS 283 Rue De La Miniere Buc, FR 78530 |
Contact | Peter Uhlir |
Correspondent | Kristine Schraufnagel GE Medical Systems, LLC 3000 North Grandview Blvd Waukesha, WI 53188 |
Product Code | JAK |
CFR Regulation Number | 892.1750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-01-26 |
Decision Date | 2018-04-24 |
Summary: | summary |