4240 DYNAMIC BP/HEART RATE MONITOR
K-Number: K914260 · 1992-09-04
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Device Summary
Frequently Asked Questions
What is the 4240 DYNAMIC BP/HEART RATE MONITOR?
4240 DYNAMIC BP/HEART RATE MONITOR is a medical device that received FDA 510(k) clearance on 1992-09-04. The listed applicant is Suntech Medical Instruments, Inc.. The 510(k) number is K914260.
When did 4240 DYNAMIC BP/HEART RATE MONITOR receive FDA 510(k) clearance?
4240 DYNAMIC BP/HEART RATE MONITOR received FDA 510(k) clearance on 1992-09-04, under 510(k) number K914260.
Who is the listed applicant for 4240 DYNAMIC BP/HEART RATE MONITOR?
The FDA 510(k) record lists Suntech Medical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 4240 DYNAMIC BP/HEART RATE MONITOR?
The FDA product code for 4240 DYNAMIC BP/HEART RATE 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 Suntech Medical Instruments, 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.
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