| Primary Device ID | 00872320003265 |
| NIH Device Record Key | 01a37a0d-88eb-4179-90e0-bbea30309b28 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pioneer Pro Wired Footswitch |
| Version Model Number | 002-00307 |
| Catalog Number | 002-00307 |
| Company DUNS | 102422578 |
| Company Name | CAO GROUP, 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 | 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 |
| Phone | 877-236-4402 |
| info@pioneerlasers.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00872320003265 [Primary] |
| GEX | Powered Laser Surgical Instrument |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-11-10 |
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