| Primary Device ID | 00811608011783 |
| NIH Device Record Key | 3fae2097-0e20-4ae8-94d2-1edce9888b51 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Volk VistaView |
| Version Model Number | VVISTAVIEW |
| Company DUNS | 071125835 |
| Company Name | VOLK OPTICAL 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 | 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00811608011783 [Primary] |
| PJZ | Camera, Ophthalmic, General-Use |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-08-19 |
| Device Publish Date | 2020-08-11 |
| 00811608011783 | VVISTAVIEW |
| 00811608013770 | VVISTAVIEW2 |