| Primary Device ID | 00744229100737 |
| NIH Device Record Key | dc0104f9-7fe0-4f88-99ba-19b12029e918 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LC Sprint |
| Version Model Number | 022F35-PRO |
| Catalog Number | na |
| Company DUNS | 804736098 |
| Company Name | PARI RESPIRATORY EQUIPMENT, INC. |
| 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 | true |
| 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 | true |
| OTC Over-The-Counter | false |