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..
Clearance details
- Applicant
- Polaroid Medical Corp.
- Product code
- Code LMC
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.