POLAROID HELIOS LASER IMAGER— 510(k) K912073
Substantially EquivalentPolaroid Medical Corp.
FDA 510(k) clearance K912073 for POLAROID HELIOS LASER IMAGER, Substantially Equivalent on 1991-08-28. Applicant: Polaroid Medical Corp.. Device class: 2.
Clearance details
- Applicant
- Polaroid Medical Corp.
- Product code
- Code LMC
- Device class
- Class 2
- Regulation
- 21 CFR 892.2040
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Recent devices under product code LMC
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