The following data is part of a premarket notification filed by Lorad Corp. with the FDA for Rhodium Filter.
Device ID | K945272 |
510k Number | K945272 |
Device Name: | RHODIUM FILTER |
Classification | System, X-ray, Mammographic |
Applicant | LORAD CORP. 36 APPLE RIDGE RD. Danbury, CT 06810 |
Contact | Marvin R Osenbaum |
Correspondent | Marvin R Osenbaum 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 | 1994-10-28 |
Decision Date | 1994-12-14 |