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FDA 510(k)

BED PATIENT MONITOR

K-Number: K854950 · 1986-03-25

Decision Date1986-03-25
Product CodeKMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BED PATIENT MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Clearview Electronics Corp.. It received FDA 510(k) clearance on 1986-03-25 under 510(k) number K854950. The device is classified under product code KMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BED PATIENT MONITOR?

BED PATIENT MONITOR is a medical device that received FDA 510(k) clearance on 1986-03-25. The listed applicant is Clearview Electronics Corp.. The 510(k) number is K854950.

When did BED PATIENT MONITOR receive FDA 510(k) clearance?

BED PATIENT MONITOR received FDA 510(k) clearance on 1986-03-25, under 510(k) number K854950.

Who is the listed applicant for BED PATIENT MONITOR?

The FDA 510(k) record lists Clearview Electronics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BED PATIENT MONITOR?

The FDA product code for BED PATIENT MONITOR is KMI.

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.

Related Devices (Code: KMI)

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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