The following data is part of a premarket notification filed by Philips Medical Systems(cleveland), Inc. with the FDA for Mr Guided Procedures (mrgp) Basic Package.
| Device ID | K983342 |
| 510k Number | K983342 |
| Device Name: | MR GUIDED PROCEDURES (MRGP) BASIC PACKAGE |
| Classification | System, Radiation Therapy, Charged-particle, Medical |
| Applicant | PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC. 595 MINER RD. Highland Heights, OH 44143 |
| Contact | Elaine K Keeler |
| Correspondent | Elaine K Keeler PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC. 595 MINER RD. Highland Heights, OH 44143 |
| Product Code | LHN |
| CFR Regulation Number | 892.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-09-23 |
| Decision Date | 1998-12-21 |
| Summary: | summary |