3 SERIES PHOTOTHERAPY CABINET— 510(k) K063621

Substantially Equivalent

Daavlin Co.

FDA 510(k) clearance K063621 for 3 SERIES PHOTOTHERAPY CABINET, Substantially Equivalent on 2007-01-17. Applicant: Daavlin Co.. Device class: 2.

Clearance details

Applicant: Daavlin Co.
Product code: Code FTC
Device class: Class 2
Regulation: 21 CFR 878.4630
Advisory panel: General, Plastic Surgery
Date received: 2006-12-05
Decision date: 2007-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bryan, OH, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FTC

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 Daavlin Co.

K930856 — PSORALITE1993-08-26
K854498 — SPECTRA 7241985-11-25
K828654 — UVB CABINET OR GOEKERMAN CABINET, MODEL SPECTRA 3051983-01-03
K827690 — SPECTRA MINI, ULTRAVIOLET EMITTER FOR DERMATOLOGICAL USE1982-10-05

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