| Primary Device ID | B741DL0 | 
| NIH Device Record Key | 5cd64018-a2c7-4c81-8cf6-d7c5f83f2b72 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Flotec | 
| Version Model Number | InGage Regulator | 
| Company DUNS | 103643730 | 
| Company Name | FLOTEC INC | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | true | 
| MRI Safety Status | MR Conditional | 
| Human Cell/Tissue Product | false | 
| Device Kit | false | 
| Device Combination Product | false | 
| Single Use | false | 
| Lot Batch | false | 
| Serial Number | true | 
| Manufacturing Date | false | 
| Expiration Date | false | 
| Donation Id Number | false | 
| Contains Natural Rubber Latex | false | 
| Labeled No Natural Rubber Latex | false | 
| RX Perscription | false | 
| OTC Over-The-Counter | false | 
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | |
| Phone | 3172736960 | 
| QA@Floteco2.com | 
| Device Issuing Agency | Device ID | 
|---|---|
| HIBCC | B741DL0 [Primary] | 
| CAN | Regulator, Pressure, Gas Cylinder | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2020-03-06 | 
| Device Publish Date | 2020-02-27 | 
| B741RW0 | RW Regulator | 
| B741MC0 | Mass Casualty Assembly | 
| B741FM0 | Flowmeter | 
| B741DL0 | InGage Regulator | 
| B741HA0 | Hose Assembly | 
| B741CH0 | Hose Assembly - Canadian Standard | 
| B741TCB0 | T.O.A.D. Connection Box | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  FLOTEC  86575482  4845267 Live/Registered | Flotec, Inc. 2015-03-25 | 
|  FLOTEC  79057474  3692710 Dead/Cancelled | BB IPR Limited 2008-04-25 | 
|  FLOTEC  77372162  not registered Dead/Abandoned | Glaxo Group Limited 2008-01-15 | 
|  FLOTEC  75201083  2286910 Live/Registered | PENTAIR FLOW TECHNOLOGIES, LLC 1996-11-20 | 
|  FLOTEC  74418120  not registered Dead/Abandoned | CIBA-GEIGY CORPORATION 1993-07-29 | 
|  FLOTEC  74126205  not registered Dead/Abandoned | Glaxo Group Limited 1990-12-21 | 
|  FLOTEC  73286741  1195014 Dead/Cancelled | Flotec Incorporated 1980-11-21 |