CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM— 510(k) K953314

Name: FDA 510(k) clearance K953314
Creator: U.S. Food and Drug Administration
Published: 1995-07-28

Substantially Equivalent

Conceptus, Inc.

FDA 510(k) clearance K953314 for CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM, Substantially Equivalent on 1995-07-28. Applicant: Conceptus, Inc.. Device class: 2.

Clearance details

Applicant: Conceptus, Inc.
Product code: Code MOV
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1995-07-12
Decision date: 1995-07-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Carlos, CA, US

Download summary PDF View on FDA.gov ↗

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