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 |