The following data is part of a premarket notification filed by Ge Medical Systems with the FDA for Signa Infinity Mr System With Excite Technology.
| Device ID | K013636 |
| 510k Number | K013636 |
| Device Name: | SIGNA INFINITY MR SYSTEM WITH EXCITE TECHNOLOGY |
| Classification | System, Nuclear Magnetic Resonance Imaging |
| Applicant | GE MEDICAL SYSTEMS P.O. BOX 414 Milwaukee, WI 53201 |
| Contact | Larry A Kroger |
| Correspondent | Larry A Kroger GE MEDICAL SYSTEMS P.O. BOX 414 Milwaukee, WI 53201 |
| Product Code | LNH |
| CFR Regulation Number | 892.1000 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-11-05 |
| Decision Date | 2002-01-24 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00840682116084 | K013636 | 000 |
| 00840682116008 | K013636 | 000 |