| Primary Device ID | 00813830026931 |
| NIH Device Record Key | fea371d2-e7c4-4a31-99bd-a0af578bde32 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pressure Relief |
| Version Model Number | 22486-FRU |
| Catalog Number | 22486-FRU |
| Company DUNS | 088302096 |
| Company Name | ACCUTRON, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00813830026931 [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 | 2023-09-25 |
| Device Publish Date | 2023-09-15 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PRESSURE RELIEF 77794891 not registered Dead/Abandoned |
Lutin, Matthew R 2009-07-31 |
![]() PRESSURE RELIEF 73225267 1149814 Dead/Cancelled |
W. R. Meadows, Inc. 1979-07-30 |
![]() PRESSURE RELIEF 72297427 0873236 Dead/Expired |
W. R. MEADOWS, INC. 1968-05-06 |