INTRAUTERINE CATHETER AND INTRODUCER— 510(k) K932993

Name: FDA 510(k) clearance K932993
Creator: U.S. Food and Drug Administration
Published: 1995-01-06

Substantially Equivalent

Conceptus, Inc.

FDA 510(k) clearance K932993 for INTRAUTERINE CATHETER AND INTRODUCER, Substantially Equivalent on 1995-01-06. Applicant: Conceptus, Inc.. Device class: 2.

Clearance details

Applicant: Conceptus, Inc.
Product code: Code MFD
Device class: Class 2
Regulation: 21 CFR 884.5250
Advisory panel: Obstetrics/Gynecology
Date received: 1993-06-18
Decision date: 1995-01-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Carlos, CA, US

Download summary PDF View on FDA.gov ↗

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