SPECTRA305— 510(k) K820492

Substantially Equivalent

Ultralite

FDA 510(k) clearance K820492 for SPECTRA305, Substantially Equivalent on 1982-03-31. Applicant: Ultralite. Device class: 2.

Clearance details

Applicant: Ultralite
Product code: Code FTC
Device class: Class 2
Regulation: 21 CFR 878.4630
Advisory panel: General, Plastic Surgery
Date received: 1982-02-23
Decision date: 1982-03-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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More clearances from Ultralite

K910091 — ULTRALITE PANELITE1991-05-30
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Data sourced from openFDA. This site is unofficial and independent of the FDA.