SOLARC/SOLRX 500 SERIES ULTRAVIOLET PHOTOTHERAPY LAMP UNIT FAMILY A NEW MEDICAL DEVICE FAMILY CONSISTING OF 5 MODELS:— 510(k) K031800

Name: FDA 510(k) clearance K031800
Creator: U.S. Food and Drug Administration
Published: 2003-09-10

Substantially Equivalent

Solarc Systems, Inc.

FDA 510(k) clearance K031800 for SOLARC/SOLRX 500 SERIES ULTRAVIOLET PHOTOTHERAPY LAMP UNIT FAMILY A NEW MEDICAL DEVICE FAMILY CONSISTING OF 5 MODELS:, Substantially Equivalent on 2003-09-10. Applicant: Solarc Systems, Inc.. Device class: 2.

Clearance details

Applicant: Solarc Systems, Inc.
Product code: Code FTC
Device class: Class 2
Regulation: 21 CFR 878.4630
Advisory panel: General, Plastic Surgery
Date received: 2003-06-11
Decision date: 2003-09-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Barrie, Ontario, CA

Download summary PDF View on FDA.gov ↗

Recent devices under product code FTC

view all

K254234 — Phototherapy System (DUV-COMBO)2026-05-01
K253871 — Klär Lite (RCW-KL1000)2026-03-04
K250425 — Ultraviolet Phototherapy Device2025-04-07
K244022 — 308nm UV Phototherapy System (4 models)2025-03-13
K242977 — 308nm Excimer Phototherapy Device (CN-308E, KN-4003B3, KN-4003B4, KN-5000C KN-5000D, KN-5000H, KN-5000K)2025-02-06

More clearances from Solarc Systems, Inc.

view all

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