PERI-PUSHER
Accelerator, Linear, Medical
DIACOR, INC.
The following data is part of a premarket notification filed by Diacor, Inc. with the FDA for Peri-pusher.
Pre-market Notification Details
| Device ID | K953046 |
| 510k Number | K953046 |
| Device Name: | PERI-PUSHER |
| Classification | Accelerator, Linear, Medical |
| 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 | IYE |
| CFR Regulation Number | 892.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-06-30 |
| Decision Date | 1995-09-22 |
Trademark Results [PERI-PUSHER]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PERI-PUSHER 75116784 2055321 Dead/Cancelled |
DIACOR, INC. 1996-06-10 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.