The following data is part of a premarket notification filed by Philips Medical Systems(cleveland), Inc. with the FDA for Infinion 0.6t Mr Imaging System.
Device ID | K013858 |
510k Number | K013858 |
Device Name: | INFINION 0.6T MR IMAGING SYSTEM |
Classification | System, Nuclear Magnetic Resonance Imaging |
Applicant | PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC. 595 MINER RD. Highland Heights, OH 44143 |
Contact | Duane C Praschan |
Correspondent | Duane C Praschan PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC. 595 MINER RD. Highland Heights, OH 44143 |
Product Code | LNH |
CFR Regulation Number | 892.1000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-11-21 |
Decision Date | 2002-01-22 |
Summary: | summary |