The following data is part of a premarket notification filed by Fischer Imaging Corp. with the FDA for Overhead Tube Mount Cascade Ii.
Device ID | K880528 |
510k Number | K880528 |
Device Name: | OVERHEAD TUBE MOUNT CASCADE II |
Classification | Tube Mount, X-ray, Diagnostic |
Applicant | FISCHER IMAGING CORP. 12300 NORTH GRANT ST. Denver, CO 80241 -3120 |
Contact | Richard Lucas |
Correspondent | Richard Lucas FISCHER IMAGING CORP. 12300 NORTH GRANT ST. Denver, CO 80241 -3120 |
Product Code | IYB |
CFR Regulation Number | 892.1770 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-02-09 |
Decision Date | 1988-02-29 |