SPECTRA305— 510(k) K820492

Substantially Equivalent

Ultralite

FDA 510(k) clearance K820492 for SPECTRA305, Substantially Equivalent on 1982-03-31. Applicant: Ultralite.

Clearance details

Applicant
Ultralite
Product code
Code FTC
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Walker, MI, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.