SD-900 OSCILLOMETRIC BP MONITOR
K-Number: K802218 · 1980-10-23
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Device Summary
Frequently Asked Questions
What is the SD-900 OSCILLOMETRIC BP MONITOR?
SD-900 OSCILLOMETRIC BP MONITOR is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Industrial & Biomedical Sensors Corp.. The 510(k) number is K802218.
When did SD-900 OSCILLOMETRIC BP MONITOR receive FDA 510(k) clearance?
SD-900 OSCILLOMETRIC BP MONITOR received FDA 510(k) clearance on 1980-10-23, under 510(k) number K802218.
Who is the listed applicant for SD-900 OSCILLOMETRIC BP MONITOR?
The FDA 510(k) record lists Industrial & Biomedical Sensors Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SD-900 OSCILLOMETRIC BP MONITOR?
The FDA product code for SD-900 OSCILLOMETRIC BP 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 Industrial & Biomedical Sensors Corp. 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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