QScreen— 510(k) K220139
Substantially EquivalentPath Medical GmbH
FDA 510(k) clearance K220139 for QScreen, Substantially Equivalent on 2022-08-03. Applicant: Path Medical GmbH. Device class: 2.
Clearance details
- Applicant
- Path Medical GmbH
- Product code
- Code GWJ
- Device class
- Class 2
- Regulation
- 21 CFR 882.1900
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Germering, DE
Recent devices under product code GWJ
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