The following data is part of a premarket notification filed by Intertech Resources, Inc. with the FDA for Flex Tube.
Device ID | K881230 |
510k Number | K881230 |
Device Name: | FLEX TUBE |
Classification | Connector, Airway (extension) |
Applicant | INTERTECH RESOURCES, INC. 5100 TICE ST. Ft. Myers, FL 33905 |
Contact | James W Pope |
Correspondent | James W Pope INTERTECH RESOURCES, INC. 5100 TICE ST. Ft. Myers, FL 33905 |
Product Code | BZA |
CFR Regulation Number | 868.5810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-03-22 |
Decision Date | 1988-04-14 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FLEX TUBE 78084923 2778651 Dead/Cancelled |
Black & Decker Corporation, The 2001-09-21 |
FLEX TUBE 76593823 3047652 Live/Registered |
Dormont Manufacturing Company 2004-05-24 |
FLEX TUBE 73226465 1165195 Dead/Cancelled |
Combustion Engineering, Inc. 1979-08-06 |