The following data is part of a premarket notification filed by Lorad Corp. with the FDA for Mammographic X-ray Unit.
Device ID | K945496 |
510k Number | K945496 |
Device Name: | MAMMOGRAPHIC X-RAY UNIT |
Classification | System, X-ray, Mammographic |
Applicant | LORAD CORP. 36 APPLE RIDGE RD. Danbury, CT 06810 |
Contact | Marvin Rosenbaum |
Correspondent | Marvin Rosenbaum LORAD CORP. 36 APPLE RIDGE RD. Danbury, CT 06810 |
Product Code | IZH |
CFR Regulation Number | 892.1710 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-11-08 |
Decision Date | 1994-12-27 |