Aneroid Type Blood Pressure Kit
K-Number: K191209 · 2019-06-18
Device Summary
Frequently Asked Questions
What is the Aneroid Type Blood Pressure Kit?
Aneroid Type Blood Pressure Kit is a medical device that received FDA 510(k) clearance on 2019-06-18. The listed applicant is Dongguan Mars Medical Products Co., Ltd.. The 510(k) number is K191209.
When did Aneroid Type Blood Pressure Kit receive FDA 510(k) clearance?
Aneroid Type Blood Pressure Kit received FDA 510(k) clearance on 2019-06-18, under 510(k) number K191209.
Who is the listed applicant for Aneroid Type Blood Pressure Kit?
The FDA 510(k) record lists Dongguan Mars Medical Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Aneroid Type Blood Pressure Kit?
The FDA product code for Aneroid Type Blood Pressure Kit is DXQ.
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.