MULTI DOPPLEX II / FETAL DOPPLEX II— 510(k) K930200

Name: FDA 510(k) clearance K930200
Creator: U.S. Food and Drug Administration
Published: 1994-06-24

Substantially Equivalent

Huntleigh Healthcare, Inc.

FDA 510(k) clearance K930200 for MULTI DOPPLEX II / FETAL DOPPLEX II, Substantially Equivalent on 1994-06-24. Applicant: Huntleigh Healthcare, Inc.. Device class: 2.

Clearance details

Applicant: Huntleigh Healthcare, Inc.
Product code: Code KNG
Device class: Class 2
Regulation: 21 CFR 884.2660
Advisory panel: Obstetrics/Gynecology
Date received: 1993-01-14
Decision date: 1994-06-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eatontown, NJ, US

Download summary PDF View on FDA.gov ↗

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