The following data is part of a premarket notification filed by Medical Advances, Inc. with the FDA for Multi Purpose Flex Array Coil : Model 235 Series.
| Device ID | K000345 |
| 510k Number | K000345 |
| Device Name: | MULTI PURPOSE FLEX ARRAY COIL : MODEL 235 SERIES |
| Classification | Coil, Magnetic Resonance, Specialty |
| Applicant | MEDICAL ADVANCES, INC. 10437 INNOVATION DR. Milwaukee, WI 53226 |
| Contact | Thomas E Tynes |
| Correspondent | Thomas E Tynes MEDICAL ADVANCES, INC. 10437 INNOVATION DR. Milwaukee, WI 53226 |
| Product Code | MOS |
| CFR Regulation Number | 892.1000 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-02-03 |
| Decision Date | 2000-04-11 |