LAPARETTE, MODEL LAP J L S H N— 510(k) K022979

Name: FDA 510(k) clearance K022979
Creator: U.S. Food and Drug Administration
Published: 2002-12-18

Substantially Equivalent

Instruments Medicaux G.B., Inc.

FDA 510(k) clearance K022979 for LAPARETTE, MODEL LAP J L S H N, Substantially Equivalent on 2002-12-18. Applicant: Instruments Medicaux G.B., Inc.. Device class: 2.

Clearance details

Applicant: Instruments Medicaux G.B., Inc.
Product code: Product code KNF
Device class: Class 2
Regulation: 21 CFR 884.4160
Advisory panel: Obstetrics/Gynecology
Date received: 2002-09-09
Decision date: 2002-12-18
Decision: Substantially Equivalent
Clearance type: Special
Location: Sherbrooke, Quebec, CA

Download summary PDF View on FDA.gov ↗

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