TRANSVAGINAL TRANSDUCER ASSEMBLY— 510(k) K900838

Name: FDA 510(k) clearance K900838
Creator: U.S. Food and Drug Administration
Published: 1990-05-23

Substantially Equivalent

Pie Medical Equipment B.V.

FDA 510(k) clearance K900838 for TRANSVAGINAL TRANSDUCER ASSEMBLY, Substantially Equivalent on 1990-05-23. Applicant: Pie Medical Equipment B.V.. Device class: 2.

Clearance details

Applicant: Pie Medical Equipment B.V.
Product code: Code HGL
Device class: Class 2
Regulation: 21 CFR 884.2960
Advisory panel: Obstetrics/Gynecology
Date received: 1990-02-22
Decision date: 1990-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Maastricht, NL

Download summary PDF View on FDA.gov ↗

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