ROSSMAX AUTOMATIC BLOOD PRESSURE MONITOR MODEL MO701K
K-Number: K060342 · 2006-04-04
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Device Summary
Frequently Asked Questions
What is the ROSSMAX AUTOMATIC BLOOD PRESSURE MONITOR MODEL MO701K?
ROSSMAX AUTOMATIC BLOOD PRESSURE MONITOR MODEL MO701K is a medical device that received FDA 510(k) clearance on 2006-04-04. The listed applicant is Rossmax International , Ltd.. The 510(k) number is K060342.
When did ROSSMAX AUTOMATIC BLOOD PRESSURE MONITOR MODEL MO701K receive FDA 510(k) clearance?
ROSSMAX AUTOMATIC BLOOD PRESSURE MONITOR MODEL MO701K received FDA 510(k) clearance on 2006-04-04, under 510(k) number K060342.
Who is the listed applicant for ROSSMAX AUTOMATIC BLOOD PRESSURE MONITOR MODEL MO701K?
The FDA 510(k) record lists Rossmax International , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ROSSMAX AUTOMATIC BLOOD PRESSURE MONITOR MODEL MO701K?
The FDA product code for ROSSMAX AUTOMATIC BLOOD PRESSURE MONITOR MODEL MO701K is DXN.
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 Rossmax International , 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: DXN)
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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