SMITH & NEPHEW RF CANNULATE — Smith & Nephew, Inc. (510(k) K090955)
SMITH & NEPHEW RF CANNULATE — Smith & Nephew, Inc. (510(k) K090955) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: SMITH & NEPHEW RF CANNULATE; Applicant: Smith & Nephew, Inc.; Clearance track: 510(k).
| Device name | SMITH & NEPHEW RF CANNULATE |
|---|---|
| Applicant | Smith & Nephew, Inc. |
| Clearance track | 510(k) |
| Submission number | K090955 |
| Decision | Substantially Equivalent |
| Decision date | 2009-07-16 |
| Date received | 2009-04-06 |
| Product code | GXI |
| Device class | 2 |
| Medical specialty | Neurology |
| Applicant location | TN, US |
| Source | openFDA device |
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$1999/mo
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