The following data is part of a premarket notification filed by Siemens Medical Systems, Inc. with the FDA for 6 Channel Body Coil.
| Device ID | K023571 |
| 510k Number | K023571 |
| Device Name: | 6 CHANNEL BODY COIL |
| Classification | Coil, Magnetic Resonance, Specialty |
| Applicant | SIEMENS MEDICAL SYSTEMS, INC. 186 WOOD AVENUE SOUTH Iselin, NJ 08830 |
| Contact | Jamie Yieh |
| Correspondent | Jamie Yieh SIEMENS MEDICAL SYSTEMS, INC. 186 WOOD AVENUE SOUTH Iselin, NJ 08830 |
| Product Code | MOS |
| CFR Regulation Number | 892.1000 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-10-24 |
| Decision Date | 2002-11-20 |
| Summary: | summary |