The following data is part of a premarket notification filed by Otech, Inc. with the FDA for Olicon Imaging Systems, Inc. Archive Systems, Nt Archive, 02archive, Archive.
Device ID | K973463 |
510k Number | K973463 |
Device Name: | OLICON IMAGING SYSTEMS, INC. ARCHIVE SYSTEMS, NT ARCHIVE, 02ARCHIVE, ARCHIVE |
Classification | Device, Digital Image Storage, Radiological |
Applicant | OTECH, INC. 6741 GRANT LN. Plano, TX 75024 |
Contact | Herman Oosterwijck |
Correspondent | Herman Oosterwijck 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 | 1997-09-12 |
Decision Date | 1997-12-02 |
Summary: | summary |