SPECTRA (ULTRAVIOLET PRODUCTS)— 510(k) K827123

Substantially Equivalent

Ultralite

FDA 510(k) clearance K827123 for SPECTRA (ULTRAVIOLET PRODUCTS), Substantially Equivalent on 1982-03-05. Applicant: Ultralite.

Clearance details

Applicant
Ultralite
Advisory panel
Unknown
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Wheatridge, CO, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.