Baylis Medical Co., Inc. · Class II · Cleared Jul 19, 2007
| K-number | K071745 |
| Device name | BAYLIS PAIN MANAGEMENT SINGLE-USE PROBE |
| Applicant | Baylis Medical Co., Inc. |
| Product code | GXI |
| Device class | Class II |
| Decision date | Jul 19, 2007 |
| Decision | Substantially Equivalent |
| Regulation | 882.4725 |
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