The following data is part of a premarket notification filed by Radiation Measurements, Inc. with the FDA for Rmi Short Distance Alignment Device.
Device ID | K885223 |
510k Number | K885223 |
Device Name: | RMI SHORT DISTANCE ALIGNMENT DEVICE |
Classification | System, Nuclear Magnetic Resonance Imaging |
Applicant | RADIATION MEASUREMENTS, INC. P.O. BOX 327 7617 DONNA DRIVE Middleton, WI 53562 |
Contact | Marie Jennaro |
Correspondent | Marie Jennaro RADIATION MEASUREMENTS, INC. P.O. BOX 327 7617 DONNA DRIVE Middleton, WI 53562 |
Product Code | LNH |
CFR Regulation Number | 892.1000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-12-20 |
Decision Date | 1989-02-17 |