| Primary Device ID | 00817495022901 |
| NIH Device Record Key | 7d9984cb-7867-477d-8e00-a13d252ffb88 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Kit, PicoWay 532 HE Resolve HP |
| Version Model Number | 7123-00-0593 |
| Company DUNS | 053468385 |
| Company Name | CANDELA CORPORATION |
| 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 | true |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| 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 |