The following data is part of a premarket notification filed by Fischer Imaging Corp. with the FDA for Micro X-50 Hf.
Device ID | K944147 |
510k Number | K944147 |
Device Name: | MICRO X-50 HF |
Classification | Generator, High-voltage, X-ray, Diagnostic |
Applicant | FISCHER IMAGING CORP. 12300 NORTH GRANT ST. Denver, CO 80241 |
Contact | James W Morgan |
Correspondent | James W Morgan FISCHER IMAGING CORP. 12300 NORTH GRANT ST. Denver, CO 80241 |
Product Code | IZO |
CFR Regulation Number | 892.1700 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-08-25 |
Decision Date | 1994-09-16 |