BATTERY POWERED ENDOSCCOPIC LIGHT SOURCE— 510(k) K960081

Name: FDA 510(k) clearance K960081
Creator: U.S. Food and Drug Administration
Published: 1996-03-12

Substantially Equivalent

Mitsubishi Cable America, Inc.

FDA 510(k) clearance K960081 for BATTERY POWERED ENDOSCCOPIC LIGHT SOURCE, Substantially Equivalent on 1996-03-12. Applicant: Mitsubishi Cable America, Inc.. Device class: 2.

Clearance details

Applicant: Mitsubishi Cable America, Inc.
Product code: Code FCQ
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1996-01-11
Decision date: 1996-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Villa Park, CA, US

Download summary PDF View on FDA.gov ↗

More clearances from Mitsubishi Cable America, Inc.

view all

K955717 — ENDOSCOPE INTRODUCER KIT1996-04-18
K936257 — ULTRATHIN FLEXIBLE ENDOSCOPE TAS-211/2.31994-03-24

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