The following data is part of a premarket notification filed by Instrumentarium Imaging, Inc. with the FDA for Mega 4 Magnetic Resonance Imaging System.
Device ID | K902044 |
510k Number | K902044 |
Device Name: | MEGA 4 MAGNETIC RESONANCE IMAGING SYSTEM |
Classification | System, Nuclear Magnetic Resonance Imaging |
Applicant | INSTRUMENTARIUM IMAGING, INC. 300 WEST EDGERTON AVE. Milwaukee, WI 53207 -6025 |
Contact | Gerry Buss |
Correspondent | Gerry Buss INSTRUMENTARIUM IMAGING, INC. 300 WEST EDGERTON AVE. Milwaukee, WI 53207 -6025 |
Product Code | LNH |
CFR Regulation Number | 892.1000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-05-07 |
Decision Date | 1990-08-23 |