| Primary Device ID | 00385640026673 |
| NIH Device Record Key | d5a86e7f-f740-4863-aa3f-b38bbe974f07 |
| Commercial Distribution Discontinuation | 2020-03-12 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Version Model Number | VT-0301-01-P |
| Company DUNS | 965484699 |
| Company Name | SUMMIT MEDICAL, 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |