Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TAKEDA MEDICAL BLOOD PRESSURE METER MODEL TM-2620

K-Number: K874339 · 1987-12-18

ApplicantA&D Engineering, Inc.
Decision Date1987-12-18
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TAKEDA MEDICAL BLOOD PRESSURE METER MODEL TM-2620 is the device name listed in this FDA 510(k) record. The listed applicant is A&D Engineering, Inc.. It received FDA 510(k) clearance on 1987-12-18 under 510(k) number K874339. The device is classified under product code DSK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAKEDA MEDICAL BLOOD PRESSURE METER MODEL TM-2620?

TAKEDA MEDICAL BLOOD PRESSURE METER MODEL TM-2620 is a medical device that received FDA 510(k) clearance on 1987-12-18. The listed applicant is A&D Engineering, Inc.. The 510(k) number is K874339.

When did TAKEDA MEDICAL BLOOD PRESSURE METER MODEL TM-2620 receive FDA 510(k) clearance?

TAKEDA MEDICAL BLOOD PRESSURE METER MODEL TM-2620 received FDA 510(k) clearance on 1987-12-18, under 510(k) number K874339.

Who is the listed applicant for TAKEDA MEDICAL BLOOD PRESSURE METER MODEL TM-2620?

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 BLOOD PRESSURE METER MODEL TM-2620?

The FDA product code for TAKEDA MEDICAL BLOOD PRESSURE METER MODEL TM-2620 is DSK.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K082734A&D MEDICAL UA-851THW DIGITAL BLOOD PRESSURE MONITORK062027A&D MEDICAL UA-789 DIGITAL BLOOD PRESSURE MONITORK061456A & D MEDICAL UM-101 DIGITAL BLOOD PRESSURE MONITORK043217A&D MEDICAL UA-767PBT DIGITAL BLOOD PRESSURE MONITORK042967A&D MEDICAL LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODELS UB-511 & UB-512K040371A & D MEDICAL UA-767BT DIGITAL BLOOD PRESSURE MONITOR

View all 34 devices →

Related Devices (Code: DSK)

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.

K231586Endophys Blood Pressure Monitor model BPM-30Endophys Technologies, LLCK160945Endophys Blood Pressure MonitorEndophys Holdings, LLCK080670MODIFICATION TO SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor MedicalK070795SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor Medical Pty, Ltd.K033738MONITORING SYSTEM, MODEL ARGUS PB-2200Schiller AGK021517ABP FOR WINDOWSRozinn Electronics, Inc.

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.

↑