Explorer Mini— 510(k) K190682
Substantially EquivalentPermobil AB
FDA 510(k) clearance K190682 for Explorer Mini, Substantially Equivalent on 2020-02-27. Applicant: Permobil AB. Device class: 2.
Clearance details
- Applicant
- Permobil AB
- Product code
- Code IPL
- Device class
- Class 2
- Regulation
- 21 CFR 890.3900
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Timra, SE
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