ANEROID SPHYGMOMANOMETER, MODEL KT-A01
K-Number: K081951 · 2008-08-15
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Device Summary
Frequently Asked Questions
What is the ANEROID SPHYGMOMANOMETER, MODEL KT-A01?
ANEROID SPHYGMOMANOMETER, MODEL KT-A01 is a medical device that received FDA 510(k) clearance on 2008-08-15. The listed applicant is Wenzhou Kindcare Import & Export Co., Ltd.. The 510(k) number is K081951.
When did ANEROID SPHYGMOMANOMETER, MODEL KT-A01 receive FDA 510(k) clearance?
ANEROID SPHYGMOMANOMETER, MODEL KT-A01 received FDA 510(k) clearance on 2008-08-15, under 510(k) number K081951.
Who is the listed applicant for ANEROID SPHYGMOMANOMETER, MODEL KT-A01?
The FDA 510(k) record lists Wenzhou Kindcare Import & Export Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANEROID SPHYGMOMANOMETER, MODEL KT-A01?
The FDA product code for ANEROID SPHYGMOMANOMETER, MODEL KT-A01 is DXQ.
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.
Related Devices (Code: DXQ)
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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