| Primary Device ID | 04560264508446 |
| NIH Device Record Key | eb7c7de4-fcfb-4bb3-81a5-0ddce88f0701 |
| Commercial Distribution Discontinuation | 2022-09-23 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FC-51 |
| Version Model Number | FC-51 |
| Company DUNS | 690710546 |
| Company Name | NAKANISHI 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 | 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 | true |
| OTC Over-The-Counter | false |