| Primary Device ID | B824SR3053M1 |
| NIH Device Record Key | aaf2dd31-7c23-44e7-b534-7c960c028d7e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SR-3053 |
| Version Model Number | M |
| Catalog Number | SR-3053-M |
| Company DUNS | 025026245 |
| Company Name | RED OAK INSTRUMENTS, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | false |
| Serial Number | false |
| 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 | true |