The following data is part of a premarket notification filed by Diacor, Inc. with the FDA for Portalcast.
Device ID | K860193 |
510k Number | K860193 |
Device Name: | PORTALCAST |
Classification | Block, Beam-shaping, Radiation Therapy |
Applicant | DIACOR, INC. 3191 SOUTH 3300 EAST, SUITE 100-A Salt Lake City, UT 84109 |
Contact | Glenn N Waterman |
Correspondent | Glenn N Waterman DIACOR, INC. 3191 SOUTH 3300 EAST, SUITE 100-A Salt Lake City, UT 84109 |
Product Code | IXI |
CFR Regulation Number | 892.5710 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-01-22 |
Decision Date | 1986-01-30 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PORTALCAST 78580353 3269422 Dead/Cancelled |
PORTALCAST, INC. 2005-03-04 |
PORTALCAST 78572128 not registered Dead/Abandoned |
PORTALCAST, INC. 2005-02-22 |
PORTALCAST 73596823 1422708 Dead/Cancelled |
DIACOR, INC. 1986-05-05 |