TUMISENSOR 1524— 510(k) K831251

Name: FDA 510(k) clearance K831251
Creator: U.S. Food and Drug Administration
Published: 1983-06-03

Substantially Equivalent

Life-Tech Intl., Inc.

FDA 510(k) clearance K831251 for TUMISENSOR 1524, Substantially Equivalent on 1983-06-03. Applicant: Life-Tech Intl., Inc.. Device class: Unclassified.

Clearance details

Applicant: Life-Tech Intl., Inc.
Product code: Code LIL
Device class: Unclassified
Advisory panel: Unknown
Date received: 1983-04-18
Decision date: 1983-06-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LIL

view all

K061676 — RIGIDOMETER, MODEL DIR-4U2006-12-27
K062042 — PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM)2006-09-06
K052929 — PREFTEST PROFESSIONAL SUITE2006-04-26
K033126 — MONARCH 21 PENILE PLETHYSMOGRAPH SYSTEM2003-10-29
K000194 — DIGITAL INFLECTION RIGIDOMETER (DIR)2000-04-10

More clearances from Life-Tech Intl., Inc.

view all

K001129 — PROLONG, MODELS PL50, PL100, PL1502000-07-06
K954505 — EZ STIM1996-12-10
K955031 — MAXISTIM1996-12-10
K954315 — PVC ABDOMINAL/RECTAL PRESSURE CATHETER1995-11-30
K954341 — URODYNAMICS TUBING AND INFUSION SETS1995-10-17

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