The following data is part of a premarket notification filed by Olicon Imaging Systems, Inc. with the FDA for Olicon Imaging Systems, Inc. 02-workstation And/or Pacsview Software.
Device ID | K973959 |
510k Number | K973959 |
Device Name: | OLICON IMAGING SYSTEMS, INC. 02-WORKSTATION AND/OR PACSVIEW SOFTWARE |
Classification | System, Digital Image Communications, Radiological |
Applicant | OLICON IMAGING SYSTEMS, INC. 6741 GRANT AVE. Plano, TX 75024 |
Contact | Herman Oosterwijck |
Correspondent | Herman Oosterwijck OLICON IMAGING SYSTEMS, INC. 6741 GRANT AVE. Plano, TX 75024 |
Product Code | LMD |
CFR Regulation Number | 892.2020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-10-16 |
Decision Date | 1997-12-22 |
Summary: | summary |