| Primary Device ID | 18622400003017 |
| NIH Device Record Key | d7ef6038-2edc-4176-a5bf-3b0e6ea4d2ce |
| Commercial Distribution Discontinuation | 2017-12-24 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Fluorotron Master |
| Version Model Number | FM-Win |
| Catalog Number | 1000-086-01 |
| Company DUNS | 807960844 |
| Company Name | OCUMETRICS 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 | false |
| Serial Number | true |
| 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 | false |