The following data is part of a premarket notification filed by Hitachi Medical Systems America, Inc. with the FDA for Hitachi Stratis, Mrh-1500 Magnetic Resonance Diagnostic Devices Version 6 Operating System Software.
Device ID | K961969 |
510k Number | K961969 |
Device Name: | HITACHI STRATIS, MRH-1500 MAGNETIC RESONANCE DIAGNOSTIC DEVICES VERSION 6 OPERATING SYSTEM SOFTWARE |
Classification | System, Nuclear Magnetic Resonance Imaging |
Applicant | HITACHI MEDICAL SYSTEMS AMERICA, INC. 1963 CASE PKWY. Twinsburg, OH 44087 |
Contact | James J Rogers |
Correspondent | James J Rogers HITACHI MEDICAL SYSTEMS AMERICA, INC. 1963 CASE PKWY. Twinsburg, OH 44087 |
Product Code | LNH |
CFR Regulation Number | 892.1000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-05-20 |
Decision Date | 1996-09-05 |
Summary: | summary |