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FDA 510(k)

SD-900 OSCILLOMETRIC BP MONITOR

K-Number: K802218 · 1980-10-23

Decision Date1980-10-23
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SD-900 OSCILLOMETRIC BP MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Industrial & Biomedical Sensors Corp.. It received FDA 510(k) clearance on 1980-10-23 under 510(k) number K802218. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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