SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313— 510(k) K760519

Name: FDA 510(k) clearance K760519
Creator: U.S. Food and Drug Administration
Published: 1976-09-03

Substantially Equivalent

Dermatron Corp.

FDA 510(k) clearance K760519 for SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313, Substantially Equivalent on 1976-09-03. Applicant: Dermatron Corp.. Device class: 2.

Clearance details

Applicant: Dermatron Corp.
Product code: Code IOB
Device class: Class 2
Regulation: 21 CFR 890.5500
Advisory panel: Physical Medicine
Date received: 1976-08-26
Decision date: 1976-09-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IOB

view all

K903660 — DERMALIGHT PSORACOMB1991-07-17
K910091 — ULTRALITE PANELITE1991-05-30
K842276 — SUNMASTER1984-07-16
K813451 — UVA FLUORESCENT TANNING LAMPS1982-01-28
K812853 — OSRAM UVA LAMP1981-12-09

More clearances from Dermatron Corp.

view all

K770862 — BLACK LAMPS,F72T12/BL/HO1977-06-27
K761094 — UVA PHOTOTHERAPY SYSTEM1976-12-02
K760471 — LAMP, FLOURESCENT BLACK, HIGH OUTPUT1976-09-15
K760482 — SUNLAMP (F40-UVB & F20-UVB)1976-09-15

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