Solarc/SolRx E-Series E720A-UVBNB-230V

• FDA 510(k) K103204 decided 27 Apr 2011 Active
• FDA GUDID UDI-DI B219E720AUVBNB230V0 listed 17 Sep 2016 Listed

1. 27 Apr 2011 Cleared FDA 510(k) K103204
2. 17 Sep 2016 Listed FDA GUDID B219E720AUVBNB230V0

Trade name

Solarc/SolRx E-Series

Generic name

Ultraviolet phototherapy unit, home-use

Model / reference

E720A-UVBNB-230V

Primary DI / UDI-DI

B219E720AUVBNB230V0

510(k) Number

K103204 ↗

FDA product code

FTC

GMDN term

Ultraviolet phototherapy unit, home-use

Device class

Class II

Regulation number

878.4630

GUDID distribution status

In Commercial Distribution

Category: Ultraviolet phototherapy unit, professional,Ultraviolet phototherapy unit, home-use

Other devices filed under FDA product code FTC (Light, Ultraviolet, Dermatological).

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• U.V. SUNLAMP (U.V. LIGHT, DERMATOLOGIC) by LIGHT SOURCES, INC.
• WALDMANN F85/100W UV21 by Sylvania Lighting Products
• PHILIPS UV-A SOLARIUM TYPE HP 3130-SUNLAMP by Philips Int'L B.V.
• Houva-NET Control System by National Biological Corp.
• FLEX CONTROLLED PHOTOTHERAPY EQUIPMENT by The Daavlin Distributing Co.
• PHOTOTHERAPEUTIX MODEL 1600B by Avex Industries, Ltd.
• SUN CAPSULE I & II SUNTANNING BOOTH by SUN CAPSULE, INC.
• PANOSOL 2000 624-616 by National Biological Corp.
• SUNBED/CANOPY, MODELS GTI 24N, 30R, 30RE & 37RE by Ecomatic GmbH, Frankfurt, F.R.G.

• Solarc/SolRx 1000-Series 1780UVB-NB

  Class II

  FDA 510(k) K935572 Active Cleared 7 Mar 1994 GUDID on market

• Solarc/SolRx E-Series E720A-UVB

  Class II

  FDA 510(k) K103204 Active Cleared 27 Apr 2011 GUDID on market

• Solarc/SolRx 500-Series 550UVB-NB-230V

  Class II

  FDA 510(k) K031800 Active Cleared 10 Sep 2003 GUDID on market

• Solarc/SolRx 100-Series 120UVB

  Class II

  FDA 510(k) K061589 Active Cleared 4 Aug 2006 GUDID on market

See all devices from Solarc Systems Inc →