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FDA 510(k)

MULTI DOPPLEX II / FETAL DOPPLEX II

K-Number: K930200 · 1994-06-24

ApplicantHuntleigh Healthcare, Inc.
Decision Date1994-06-24
Product CodeKNG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MULTI DOPPLEX II / FETAL DOPPLEX II is the device name listed in this FDA 510(k) record. The listed applicant is Huntleigh Healthcare, Inc.. It received FDA 510(k) clearance on 1994-06-24 under 510(k) number K930200. The device is classified under product code KNG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI DOPPLEX II / FETAL DOPPLEX II?

MULTI DOPPLEX II / FETAL DOPPLEX II is a medical device that received FDA 510(k) clearance on 1994-06-24. The listed applicant is Huntleigh Healthcare, Inc.. The 510(k) number is K930200.

When did MULTI DOPPLEX II / FETAL DOPPLEX II receive FDA 510(k) clearance?

MULTI DOPPLEX II / FETAL DOPPLEX II received FDA 510(k) clearance on 1994-06-24, under 510(k) number K930200.

Who is the listed applicant for MULTI DOPPLEX II / FETAL DOPPLEX II?

The FDA 510(k) record lists Huntleigh Healthcare, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTI DOPPLEX II / FETAL DOPPLEX II?

The FDA product code for MULTI DOPPLEX II / FETAL DOPPLEX II is KNG.

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Other records listing Huntleigh Healthcare, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K032315IOP8 INTRA OPERATIVE PROBEK022786DVT60K010744FLOWTRON UNIVERSAL, MODEL AC600K012008STS RANGE , MODELS STS20,STS30,STS40K002186VASCULAR ASSISTK010894BABY DOPPLEX 3002 (BD3002)

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Related Devices (Code: KNG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252669Fetal Doppler U8-25, U9-25Zhongshan Xiaolan Town Senlan Electronic FactoryK242846Doppler FHR Detector (BF-500D+, BF-560)Shenzhen Bestman Instrument Co., Ltd.K233823Ultrasonic Fetal DopplerShenzhen Jamr Technology Co., Ltd.K232893Pocket Fetal Doppler (CONTEC 10D), Pocket Fetal Doppler (CONTEC 10E), Pocket Fetal Doppler (CONTEC 10F)Contec Medical Systems Co.,LtdK220245Pocket Fetal Doppler (Models CONTEC10C and CONTEC10CL)Contec Medical Systems Co.,LtdK211940Fetal DopplerShenzhen Taikang Medical Equipment Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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