TAKEDA MEDICAL AUTO. DIGITAL BLOOD PRES. MONITOR
K-Number: K882824 · 1989-01-17
Advertisement
Device Summary
Frequently Asked Questions
What is the TAKEDA MEDICAL AUTO. DIGITAL BLOOD PRES. MONITOR?
TAKEDA MEDICAL AUTO. DIGITAL BLOOD PRES. MONITOR is a medical device that received FDA 510(k) clearance on 1989-01-17. The listed applicant is A&D Engineering, Inc.. The 510(k) number is K882824.
When did TAKEDA MEDICAL AUTO. DIGITAL BLOOD PRES. MONITOR receive FDA 510(k) clearance?
TAKEDA MEDICAL AUTO. DIGITAL BLOOD PRES. MONITOR received FDA 510(k) clearance on 1989-01-17, under 510(k) number K882824.
Who is the listed applicant for TAKEDA MEDICAL AUTO. DIGITAL BLOOD PRES. MONITOR?
The FDA 510(k) record lists A&D Engineering, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TAKEDA MEDICAL AUTO. DIGITAL BLOOD PRES. MONITOR?
The FDA product code for TAKEDA MEDICAL AUTO. DIGITAL BLOOD PRES. MONITOR 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 A&D Engineering, Inc. 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.
Advertisement