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FDA 510(k)

PD-100 SERIES ULTRASONIC POCKET DOPPLER

K-Number: K111934 · 2011-09-22

ApplicantAdvanced Instrumentations, Inc.
Decision Date2011-09-22
Product CodeKNG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PD-100 SERIES ULTRASONIC POCKET DOPPLER is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Instrumentations, Inc.. It received FDA 510(k) clearance on 2011-09-22 under 510(k) number K111934. 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 PD-100 SERIES ULTRASONIC POCKET DOPPLER?

PD-100 SERIES ULTRASONIC POCKET DOPPLER is a medical device that received FDA 510(k) clearance on 2011-09-22. The listed applicant is Advanced Instrumentations, Inc.. The 510(k) number is K111934.

When did PD-100 SERIES ULTRASONIC POCKET DOPPLER receive FDA 510(k) clearance?

PD-100 SERIES ULTRASONIC POCKET DOPPLER received FDA 510(k) clearance on 2011-09-22, under 510(k) number K111934.

Who is the listed applicant for PD-100 SERIES ULTRASONIC POCKET DOPPLER?

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

What is the FDA product code for PD-100 SERIES ULTRASONIC POCKET DOPPLER?

The FDA product code for PD-100 SERIES ULTRASONIC POCKET DOPPLER is KNG.

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Other records listing Advanced Instrumentations, 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.

K172931DUS-6000 Digital Ultrasonic Diagnostic Imaging SystemK172055DUS-7000 Digital Color Doppler Ultrasound SystemK132059DIAGNOSTIC ULTRASOUND SYSTEMK123048PATIENT MONITOR MODELS PM-2000A, PM-2000A+, PM-2000A PROK120075AM-6000 ANESTHESIA MACHINEK112317FM-9000 PLUS FETAL AND MATERNAL MONITOR

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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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