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FDA 510(k)

BED PATIENT PRESENCE MONITOR

K-Number: K871203 · 1987-05-26

ApplicantHuman Technologies, Inc.
Decision Date1987-05-26
Product CodeKMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BED PATIENT PRESENCE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Human Technologies, Inc.. It received FDA 510(k) clearance on 1987-05-26 under 510(k) number K871203. 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 PRESENCE MONITOR?

BED PATIENT PRESENCE MONITOR is a medical device that received FDA 510(k) clearance on 1987-05-26. The listed applicant is Human Technologies, Inc.. The 510(k) number is K871203.

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

BED PATIENT PRESENCE MONITOR received FDA 510(k) clearance on 1987-05-26, under 510(k) number K871203.

Who is the listed applicant for BED PATIENT PRESENCE MONITOR?

The FDA 510(k) record lists Human Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BED PATIENT PRESENCE MONITOR?

The FDA product code for BED PATIENT PRESENCE 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.

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Other records listing Human Technologies, 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.

K880639ACCUTEMP(TM) TEMP. MONITIORING SYSTEM SWALLOWABLEK871158SIBIS REMOTE ACTUATOR

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.

K131585INTEL-GE CARE INNOVATIONS QUIETCAREIntel-Ge Care Innovations, LLCK130752DYNASENSE SYSTEMCentauri Medical, Inc.K101109VIVATRAKWireless Medcare, LLCK090138MOBILECARE MONITOR, MODEL 2100Aframe Digital, Inc.K942770ULTIMAT-SENSOR FOR BED OCCUPANCY MONITORUltimate Development Corp.K943481INFORMER PLUSMicro-Tech Medical, 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.

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