The following data is part of a premarket notification filed by Otech, Inc. with the FDA for Wise Image Management System.
Device ID | K971451 |
510k Number | K971451 |
Device Name: | WISE IMAGE MANAGEMENT SYSTEM |
Classification | Device, Digital Image Storage, Radiological |
Applicant | OTECH, INC. 6741 GRANT LN. Plano, TX 75024 |
Contact | Herman Oosterwijk |
Correspondent | Herman Oosterwijk OTECH, INC. 6741 GRANT LN. Plano, TX 75024 |
Product Code | LMB |
CFR Regulation Number | 892.2010 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-04-21 |
Decision Date | 1997-06-26 |
Summary: | summary |