The following data is part of a premarket notification filed by Medical Advances, Inc. with the FDA for Model 4050-64; 5.25 & 4065-64; 6.50 Loop Coil.
Device ID | K901639 |
510k Number | K901639 |
Device Name: | MODEL 4050-64; 5.25 & 4065-64; 6.50 LOOP COIL |
Classification | System, Nuclear Magnetic Resonance Imaging |
Applicant | MEDICAL ADVANCES, INC. 10431 W. WATERTOWN PLANK RD. P.O. BOX 26425 Milwaukee, WI 53226 -0425 |
Contact | William L Zabriskie |
Correspondent | William L Zabriskie MEDICAL ADVANCES, INC. 10431 W. WATERTOWN PLANK RD. P.O. BOX 26425 Milwaukee, WI 53226 -0425 |
Product Code | LNH |
CFR Regulation Number | 892.1000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-04-09 |
Decision Date | 1990-05-14 |