POLAROID HELIOS LASER IMAGER— 510(k) K912073

Substantially Equivalent

Polaroid 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
Download summary PDFView on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.