OncoPatch— 510(k) K252296
Substantially EquivalentOncopatch, Inc.
FDA 510(k) clearance K252296 for OncoPatch, Substantially Equivalent on 2025-12-05. Applicant: Oncopatch, Inc.. Device class: 2.
Clearance details
- Applicant
- Oncopatch, Inc.
- Product code
- Code KXK
- Device class
- Class 2
- Regulation
- 21 CFR 892.5730
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Aurora, CO, US
Recent devices under product code KXK
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