The following data is part of a premarket notification filed by Hitachi Medical Systems America, Inc. with the FDA for Echelon Mr-rcc-150 Cardiac Coil.
Device ID | K063513 |
510k Number | K063513 |
Device Name: | ECHELON MR-RCC-150 CARDIAC COIL |
Classification | Coil, Magnetic Resonance, Specialty |
Applicant | HITACHI MEDICAL SYSTEMS AMERICA, INC. 1959 SUMMIT COMMERCE PARK Twinsburg, OH 44080 |
Contact | Douglas J Thistlewaite |
Correspondent | Douglas J Thistlewaite HITACHI MEDICAL SYSTEMS AMERICA, INC. 1959 SUMMIT COMMERCE PARK Twinsburg, OH 44080 |
Product Code | MOS |
CFR Regulation Number | 892.1000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-11-21 |
Decision Date | 2006-12-12 |
Summary: | summary |