The following data is part of a premarket notification filed by Olympus with the FDA for Olympus Imagemanagersystem.
Device ID | K934888 |
510k Number | K934888 |
Device Name: | OLYMPUS IMAGEMANAGERSYSTEM |
Classification | Device, Digital Image Storage, Radiological |
Applicant | OLYMPUS 4 NEVADA DR. Lake Success, NY 11042 -1179 |
Contact | Barry E Sands |
Correspondent | Barry E Sands OLYMPUS 4 NEVADA DR. Lake Success, NY 11042 -1179 |
Product Code | LMB |
CFR Regulation Number | 892.2010 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-10-13 |
Decision Date | 1994-01-25 |