PBN FALLOPIAN TUBE CATHETER SYSTEM— 510(k) K000620

Name: FDA 510(k) clearance K000620
Creator: U.S. Food and Drug Administration
Published: 2000-10-30

Substantially Equivalent

Medical Device Technologies, Inc.

FDA 510(k) clearance K000620 for PBN FALLOPIAN TUBE CATHETER SYSTEM, Substantially Equivalent on 2000-10-30. Applicant: Medical Device Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Medical Device Technologies, Inc.
Product code: Code MDG
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 2000-02-24
Decision date: 2000-10-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gainesville, FL, US

Download summary PDF View on FDA.gov ↗

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