MODEL PC-860 FETAL DOPPLER
K-Number: K082055 · 2009-02-06
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Device Summary
Frequently Asked Questions
What is the MODEL PC-860 FETAL DOPPLER?
MODEL PC-860 FETAL DOPPLER is a medical device that received FDA 510(k) clearance on 2009-02-06. The listed applicant is Shenzhen Creative Industry Co., Ltd.. The 510(k) number is K082055.
When did MODEL PC-860 FETAL DOPPLER receive FDA 510(k) clearance?
MODEL PC-860 FETAL DOPPLER received FDA 510(k) clearance on 2009-02-06, under 510(k) number K082055.
Who is the listed applicant for MODEL PC-860 FETAL DOPPLER?
The FDA 510(k) record lists Shenzhen Creative Industry Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL PC-860 FETAL DOPPLER?
The FDA product code for MODEL PC-860 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 Shenzhen Creative Industry 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.
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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