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FDA 510(k)

MOSS LIMB LOAD MONITOR LM101-1

K-Number: K844202 · 1984-11-27

ApplicantMoss Rehabilation Hospital
Decision Date1984-11-27
Product CodeIKE
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MOSS LIMB LOAD MONITOR LM101-1 is the device name listed in this FDA 510(k) record. The listed applicant is Moss Rehabilation Hospital. It received FDA 510(k) clearance on 1984-11-27 under 510(k) number K844202. The device is classified under product code IKE. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOSS LIMB LOAD MONITOR LM101-1?

MOSS LIMB LOAD MONITOR LM101-1 is a medical device that received FDA 510(k) clearance on 1984-11-27. The listed applicant is Moss Rehabilation Hospital. The 510(k) number is K844202.

When did MOSS LIMB LOAD MONITOR LM101-1 receive FDA 510(k) clearance?

MOSS LIMB LOAD MONITOR LM101-1 received FDA 510(k) clearance on 1984-11-27, under 510(k) number K844202.

Who is the listed applicant for MOSS LIMB LOAD MONITOR LM101-1?

The FDA 510(k) record lists Moss Rehabilation Hospital as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOSS LIMB LOAD MONITOR LM101-1?

The FDA product code for MOSS LIMB LOAD MONITOR LM101-1 is IKE.

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Related Devices (Code: IKE)

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.

K060125SONIC PALPOMETERPalpometer Systems, Inc.K954670PRESSORE MONITORCleveland Medical Devices, Inc.K915369THE EQUALIZERAdvanced Rehabilitative Technology, Inc.K915326PORTABLE LIMB LOAD MONITOR (BMLLM-100)Bar Med Pty , Ltd.K920091IOWA ORAL PERFORMANCE ISNTRUMENTBreakthrough, Inc.K915897FPLWrm Computers

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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