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FDA 510(k)

FOOT WEIGHT ALARM

K-Number: K962591 · 1996-12-04

ApplicantCleveland Medical Devices, Inc.
Decision Date1996-12-04
Product CodeIRN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FOOT WEIGHT ALARM is the device name listed in this FDA 510(k) record. The listed applicant is Cleveland Medical Devices, Inc.. It received FDA 510(k) clearance on 1996-12-04 under 510(k) number K962591. The device is classified under product code IRN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOOT WEIGHT ALARM?

FOOT WEIGHT ALARM is a medical device that received FDA 510(k) clearance on 1996-12-04. The listed applicant is Cleveland Medical Devices, Inc.. The 510(k) number is K962591.

When did FOOT WEIGHT ALARM receive FDA 510(k) clearance?

FOOT WEIGHT ALARM received FDA 510(k) clearance on 1996-12-04, under 510(k) number K962591.

Who is the listed applicant for FOOT WEIGHT ALARM?

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

What is the FDA product code for FOOT WEIGHT ALARM?

The FDA product code for FOOT WEIGHT ALARM is IRN.

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Other records listing Cleveland Medical Devices, 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.

K063872KINESIAK042039FAMILY OF CRYSTAL 20 MONITORS MODEL #CS20-600,900,1300,1400,2400 & 120K013863CRYSTAL MONITOR MODEL 16K001110CRYSTAL-EEG MODEL 15K970672CRYSTAL-EEG MODEL 10 (MODEL 10)K964690LIBERTY VALVE

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Related Devices (Code: IRN)

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.

K060150SMARTSTEP SYSTEM/SMARSTEP CLINIC SYSTEMAndante Medical Devices , Ltd.K023161SMARTSTEP SYSTEMAndante Medical Device, Ltd.K991313ACCUTRED SHOEOrthopedic Technology Research, Inc.K960307INDEX SHOEOrthopedic Technology Research, Inc.K955034FORCEGUARDImpact Monitors, Inc.K950656PED ALERTOrbitec Technologies Corp.

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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