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FDA 510(k)

MONITOR, BED, TECHNOLICS

K-Number: K770695 · 1977-07-14

ApplicantTechnolics, Inc.
Decision Date1977-07-14
Product CodeKMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MONITOR, BED, TECHNOLICS is the device name listed in this FDA 510(k) record. The listed applicant is Technolics, Inc.. It received FDA 510(k) clearance on 1977-07-14 under 510(k) number K770695. 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 MONITOR, BED, TECHNOLICS?

MONITOR, BED, TECHNOLICS is a medical device that received FDA 510(k) clearance on 1977-07-14. The listed applicant is Technolics, Inc.. The 510(k) number is K770695.

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

MONITOR, BED, TECHNOLICS received FDA 510(k) clearance on 1977-07-14, under 510(k) number K770695.

Who is the listed applicant for MONITOR, BED, TECHNOLICS?

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

What is the FDA product code for MONITOR, BED, TECHNOLICS?

The FDA product code for MONITOR, BED, TECHNOLICS is KMI.

Related Clinical Trials

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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

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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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