The following data is part of a premarket notification filed by Ralco S.r.l. with the FDA for Ralco, Model R225 Acs.
Device ID | K091517 |
510k Number | K091517 |
Device Name: | RALCO, MODEL R225 ACS |
Classification | Collimator, Automatic, Radiographic |
Applicant | RALCO S.R.L. 333 MILFORD ROAD Deerfield, IL 60015 |
Contact | Daniel Kamm |
Correspondent | Daniel Kamm RALCO S.R.L. 333 MILFORD ROAD Deerfield, IL 60015 |
Product Code | IZW |
CFR Regulation Number | 892.1610 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-05-22 |
Decision Date | 2009-07-14 |
Summary: | summary |