INIVOX ELECTRODE/CATHETER SYS— 510(k) K832916

Name: FDA 510(k) clearance K832916
Creator: U.S. Food and Drug Administration
Published: 1983-11-14

Substantially Equivalent

Critikon Company, LLC

FDA 510(k) clearance K832916 for INIVOX ELECTRODE/CATHETER SYS, Substantially Equivalent on 1983-11-14. Applicant: Critikon Company, LLC. Device class: 3.

Clearance details

Applicant: Critikon Company, LLC
Product code: Code LLE
Device class: Class 3
Advisory panel: Unknown
Date received: 1983-08-29
Decision date: 1983-11-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LLE

view all

K833430 — BLOOD GAS EXPERSYSTEM 87001984-02-10

More clearances from Critikon Company, LLC

view all

K002248 — DINAMAP PRO 1000 MONITOR, MODEL 10002000-09-21
K000500 — DINAMAP ADVANCED NIBP MODULE2000-05-26
K992638 — DINAMAP PRO SERIES MONITOR, MODELS 100, 200, 300, 4002000-02-24
K982342 — DINAMAP MPS SELECT PORTABLE MONITOR1998-08-14
K943709 — DINAMAP PLUS VITAL SIGNS MONOITOR1995-06-16

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