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FDA 510(k)

FETAL DOPPLER

K-Number: K112911 · 2011-10-27

Decision Date2011-10-27
Product CodeKNG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FETAL DOPPLER is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Choice Electronic Technololgy Co., Ltd.. It received FDA 510(k) clearance on 2011-10-27 under 510(k) number K112911. 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 FETAL DOPPLER?

FETAL DOPPLER is a medical device that received FDA 510(k) clearance on 2011-10-27. The listed applicant is Beijing Choice Electronic Technololgy Co., Ltd.. The 510(k) number is K112911.

When did FETAL DOPPLER receive FDA 510(k) clearance?

FETAL DOPPLER received FDA 510(k) clearance on 2011-10-27, under 510(k) number K112911.

Who is the listed applicant for FETAL DOPPLER?

The FDA 510(k) record lists Beijing Choice Electronic Technololgy Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FETAL DOPPLER?

The FDA product code for FETAL DOPPLER is KNG.

Related Clinical Trials

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.

Other records listing Beijing Choice Electronic Technololgy Co., Ltd. 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.

View all 24 devices →

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.

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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