PORTALCAST
Block, Beam-shaping, Radiation Therapy
DIACOR, INC.
The following data is part of a premarket notification filed by Diacor, Inc. with the FDA for Portalcast.
Pre-market Notification Details
| 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 |
Trademark Results [PORTALCAST]
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 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.