FIBER OPTIC ADAPTERS#60-0893— 510(k) K810300

Name: FDA 510(k) clearance K810300
Creator: U.S. Food and Drug Administration
Published: 1981-02-27

Substantially Equivalent

Aspen Laboratories, Inc.

FDA 510(k) clearance K810300 for FIBER OPTIC ADAPTERS#60-0893, Substantially Equivalent on 1981-02-27. Applicant: Aspen Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Aspen Laboratories, Inc.
Product code: Code HBI
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 1981-02-03
Decision date: 1981-02-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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 Aspen Laboratories, Inc.

view all

K981220 — SYSTEM 7500 ABC ELECTROSURGICAL UNIT1998-04-21
K963088 — SHEATH, ELECTROSURGICAL PENCIL1996-09-13
K955834 — SYSTEM 6500 ABC ELECTROSURGICAL UNIT1996-07-11
K960296 — 4000 ETM1996-02-20
K953081 — BEAMER PLUS1995-10-30

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