V12 PRO— 510(k) K210913
Substantially EquivalentSlk Medical GmbH
FDA 510(k) clearance K210913 for V12 PRO, Substantially Equivalent on 2021-08-04. Applicant: Slk Medical GmbH. Device class: 2.
Clearance details
- Applicant
- Slk Medical GmbH
- Product code
- Code IRP
- Device class
- Class 2
- Regulation
- 21 CFR 890.5650
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Waltrop, DE
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