The following data is part of a premarket notification filed by Omega Medical Imaging, Inc. with the FDA for E-view Fluoroscopy System, Model Cs-50.
Device ID | K062647 |
510k Number | K062647 |
Device Name: | E-VIEW FLUOROSCOPY SYSTEM, MODEL CS-50 |
Classification | Interventional Fluoroscopic X-ray System |
Applicant | OMEGA MEDICAL IMAGING, INC. 675 HICKMAN CIRCLE Sanford, FL 32771 |
Contact | James A Princehorn |
Correspondent | James A Princehorn OMEGA MEDICAL IMAGING, INC. 675 HICKMAN CIRCLE Sanford, FL 32771 |
Product Code | OWB |
CFR Regulation Number | 892.1650 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-09-06 |
Decision Date | 2006-10-20 |
Summary: | summary |