ECHOMARK INTRAUTERINE GUIDING CATHETER— 510(k) K932436

Name: FDA 510(k) clearance K932436
Creator: U.S. Food and Drug Administration
Published: 1995-11-16

Substantially Equivalent

Echocath, Inc.

FDA 510(k) clearance K932436 for ECHOMARK INTRAUTERINE GUIDING CATHETER, Substantially Equivalent on 1995-11-16. Applicant: Echocath, Inc.. Device class: 2.

Clearance details

Applicant: Echocath, Inc.
Product code: Code MOV
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1993-05-19
Decision date: 1995-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Princeton, NJ, US

Download summary PDF View on FDA.gov ↗

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