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FDA 510(k)

CADENCE DOPPLER ULTRASOUND SYSTEM

K-Number: K991441 · 1999-12-28

ApplicantMedasonics, Inc.
Decision Date1999-12-28
Product CodeKNG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CADENCE DOPPLER ULTRASOUND SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medasonics, Inc.. It received FDA 510(k) clearance on 1999-12-28 under 510(k) number K991441. 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 CADENCE DOPPLER ULTRASOUND SYSTEM?

CADENCE DOPPLER ULTRASOUND SYSTEM is a medical device that received FDA 510(k) clearance on 1999-12-28. The listed applicant is Medasonics, Inc.. The 510(k) number is K991441.

When did CADENCE DOPPLER ULTRASOUND SYSTEM receive FDA 510(k) clearance?

CADENCE DOPPLER ULTRASOUND SYSTEM received FDA 510(k) clearance on 1999-12-28, under 510(k) number K991441.

Who is the listed applicant for CADENCE DOPPLER ULTRASOUND SYSTEM?

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

What is the FDA product code for CADENCE DOPPLER ULTRASOUND SYSTEM?

The FDA product code for CADENCE DOPPLER ULTRASOUND SYSTEM is KNG.

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Other records listing Medasonics, 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.

K962796NEUROGUARD TRANSCRANIAL DOPPLER ULTRASOUND SYSTEMK961116FIRST BEAT/CARDIO BEAT/CALCK914862CEREBROVASCULAR DIAGNOSTIC SYSTEM; CDSK911453OBTRASOUND STETHOSCOPE FETAL CALCK882018MEDACORD PVL, PERSONAL VASCULAR LABORATORYK872292TRANSPECT TRANSCRANIAL DOPPLER

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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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