The following data is part of a premarket notification filed by Ge Medical Systems, Llc with the FDA for Discovery Mr750 3.0t.
| Device ID | K142361 |
| 510k Number | K142361 |
| Device Name: | Discovery MR750 3.0T |
| Classification | System, Nuclear Magnetic Resonance Imaging |
| Applicant | GE MEDICAL SYSTEMS, LLC 3200 N. GRANDVIEW BLVD. Waukesha, WI 53188 |
| Contact | Jenny Wong |
| Correspondent | Jenny Wong GE MEDICAL SYSTEMS, LLC 3200 N. GRANDVIEW BLVD. Waukesha, WI 53188 |
| Product Code | LNH |
| CFR Regulation Number | 892.1000 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-08-25 |
| Decision Date | 2014-12-05 |
| Summary: | summary |