510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K930200Substantially Equivalent

Multi Dopplex II / Fetal Dopplex II

Huntleigh Healthcare Ltd., Eatontown NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930200 is the FDA 510(k) clearance record for MULTI DOPPLEX II / FETAL DOPPLEX II, a class II device, cleared for Huntleigh Healthcare, Inc. on under FDA product code KNG (Monitor, Ultrasonic, Fetal). FDA records list 27 510(k) clearances for Huntleigh Healthcare, Inc., from to . As of , FDA records show no recalls naming K930200.

Clearance record

Decision date
Received
(526 days to decision)
Product code
KNG Monitor, Ultrasonic, Fetal
Regulation
21 CFR 884.2660
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Huntleigh Healthcare, Inc. 40 Christopher Way, Eatontown NJ
510(k) summary
Statement
Third party review
No

Clearances, product code KNG

Trailing 12 months
1 clearance under product code KNG in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code KNG, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260