NEXTEC FIBEROPTIC ILLUMINAT 150 WATT/HALO/3500 KEL— 510(k) K920167

Name: FDA 510(k) clearance K920167
Creator: U.S. Food and Drug Administration
Published: 1992-03-23

Substantially Equivalent

Nextec Corp.

FDA 510(k) clearance K920167 for NEXTEC FIBEROPTIC ILLUMINAT 150 WATT/HALO/3500 KEL, Substantially Equivalent on 1992-03-23. Applicant: Nextec Corp.. Device class: 2.

Clearance details

Applicant: Nextec Corp.
Product code: Code HBI
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 1992-01-10
Decision date: 1992-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Naples, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HBI

view all

K223183 — Light-Guide Cables2023-01-13
K163185 — OptiLux LED Illuminator2016-11-21
K141781 — KOGENT SPETZLER LIGHTED SUCTION TUBES2015-04-09
K111342 — LIGHT GUIDE CABLE2011-11-25
K052979 — 1125 XSB XENON FIBER-OPTIC LIGHT SOURCE2005-10-31

More clearances from Nextec Corp.

view all

K922462 — NEXTEC FIBEROPTIC CABLES1992-09-21
K921646 — NEXTEC FIBEROPTIC ILLUMINATOR 300 WATT XENON1992-05-13

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