The following data is part of a premarket notification filed by Burron Medical Products, Inc. with the FDA for Clean-flush.
| Device ID | K830572 |
| 510k Number | K830572 |
| Device Name: | CLEAN-FLUSH |
| Classification | Syringe, Irrigating (non Dental) |
| Applicant | BURRON MEDICAL PRODUCTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KYZ |
| CFR Regulation Number | 880.6960 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-02-23 |
| Decision Date | 1983-03-17 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CLEAN-FLUSH 86085728 4550859 Live/Registered |
Aircraft Technologies, Inc. 2013-10-08 |
![]() CLEAN-FLUSH 77055010 3421256 Dead/Cancelled |
Aircraft Technologies, Inc. 2006-12-01 |
![]() CLEAN-FLUSH 75631371 2420565 Live/Registered |
Aircraft Technologies, Inc. 1999-02-01 |
![]() CLEAN-FLUSH 72409981 0947759 Dead/Expired |
SHERWOOD PRODUCTS 1971-12-10 |