The following data is part of a premarket notification filed by General Electric Co. with the FDA for Advantage V.s. Ct/mr Rad Diagnostic Workstation.
Device ID | K913770 |
510k Number | K913770 |
Device Name: | ADVANTAGE V.S. CT/MR RAD DIAGNOSTIC WORKSTATION |
Classification | System, Nuclear Magnetic Resonance Imaging |
Applicant | GENERAL ELECTRIC CO. P.O. BOX 414 Milwaukee, WI 53201 |
Contact | Larry A Kroger |
Correspondent | Larry A Kroger GENERAL ELECTRIC CO. P.O. BOX 414 Milwaukee, WI 53201 |
Product Code | LNH |
CFR Regulation Number | 892.1000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-08-22 |
Decision Date | 1991-12-27 |