PIM 1.0 LASER DOPPLER PERFUSION IMAGER— 510(k) K920844
Substantially EquivalentLisca Development AB
FDA 510(k) clearance K920844 for PIM 1.0 LASER DOPPLER PERFUSION IMAGER, Substantially Equivalent on 1992-07-21. Applicant: Lisca Development AB. Device class: 2.
Clearance details
- Applicant
- Lisca Development AB
- Product code
- Product code DPW
- Device class
- Class 2
- Regulation
- 21 CFR 870.2100
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Linkoping, SE
Recent devices under product code DPW
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