The following data is part of a premarket notification filed by Radiology Information Systems, Inc. with the FDA for Ris Scanview System (rsvs).
Device ID | K970641 |
510k Number | K970641 |
Device Name: | RIS SCANVIEW SYSTEM (RSVS) |
Classification | System, Digital Image Communications, Radiological |
Applicant | RADIOLOGY INFORMATION SYSTEMS, INC. 2004 ADAMS HILL RD. Vienna, VA 22182 |
Contact | Joe S Pi |
Correspondent | Joe S Pi RADIOLOGY INFORMATION SYSTEMS, INC. 2004 ADAMS HILL RD. Vienna, VA 22182 |
Product Code | LMD |
CFR Regulation Number | 892.2020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-02-20 |
Decision Date | 1997-05-02 |
Summary: | summary |