The following data is part of a premarket notification filed by Usa Instruments, Inc. with the FDA for Spirit Iii Totalsense Cardiac Coil.
| Device ID | K031172 |
| 510k Number | K031172 |
| Device Name: | SPIRIT III TOTALSENSE CARDIAC COIL |
| Classification | Coil, Magnetic Resonance, Specialty |
| Applicant | USA INSTRUMENTS, INC. 1515 DANNER DR. Aurora, OH 44202 |
| Contact | Christie Shumaker |
| Correspondent | Christie Shumaker USA INSTRUMENTS, INC. 1515 DANNER DR. Aurora, OH 44202 |
| Product Code | MOS |
| CFR Regulation Number | 892.1000 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-04-14 |
| Decision Date | 2003-05-29 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00840682116473 | K031172 | 000 |