The following data is part of a premarket notification filed by Riverpoint Medical with the FDA for Brachytherapy Needles, Rp Sleeve, Rp Brachy-spacer, Gold Makers.
Device ID | K103449 |
510k Number | K103449 |
Device Name: | BRACHYTHERAPY NEEDLES, RP SLEEVE, RP BRACHY-SPACER, GOLD MAKERS |
Classification | Source, Brachytherapy, Radionuclide |
Applicant | RIVERPOINT MEDICAL 825 NE 25TH AVE. Portland, OR 97232 |
Contact | Doug Rowley |
Correspondent | Doug Rowley RIVERPOINT MEDICAL 825 NE 25TH AVE. Portland, OR 97232 |
Product Code | KXK |
CFR Regulation Number | 892.5730 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-11-23 |
Decision Date | 2011-02-25 |
Summary: | summary |