Compound W Wart Removal System Dual Power— 510(k) K161294
Substantially EquivalentMedtech Products, Inc.
FDA 510(k) clearance K161294 for Compound W Wart Removal System Dual Power, Substantially Equivalent on 2016-09-15. Applicant: Medtech Products, Inc.. Device class: 2.
Clearance details
- Applicant
- Medtech Products, Inc.
- Product code
- Code GEH
- Device class
- Class 2
- Regulation
- 21 CFR 878.4350
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tarrytown, NY, US
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More clearances from Medtech Products, Inc.
view allAdverse events under product code GEH
product code GEH- Death
- 25
- Injury
- 351
- Malfunction
- 901
- Total
- 1,277
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.