ULTRALITE PANELITE— 510(k) K910091

Substantially Equivalent

Ultralite

FDA 510(k) clearance K910091 for ULTRALITE PANELITE, Substantially Equivalent on 1991-05-30. Applicant: Ultralite. Device class: 2.

Clearance details

Applicant: Ultralite
Product code: Code IOB
Device class: Class 2
Regulation: 21 CFR 890.5500
Advisory panel: Physical Medicine
Date received: 1991-01-09
Decision date: 1991-05-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lawrenceville, GA, US

Download summary PDF View on FDA.gov ↗

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K761179 — PSORALITE1977-05-03

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