FDA 510(k)

CADWELL LIMB MOVEMENT MODULE

K-Number: K040986 · 2004-07-01

Decision Date2004-07-01

Product CodeLEL

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

CADWELL LIMB MOVEMENT MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Cadwell Laboratories, Inc.. It received FDA 510(k) clearance on 2004-07-01 under 510(k) number K040986. The device is classified under product code LEL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CADWELL LIMB MOVEMENT MODULE?

CADWELL LIMB MOVEMENT MODULE is a medical device that received FDA 510(k) clearance on 2004-07-01. The listed applicant is Cadwell Laboratories, Inc.. The 510(k) number is K040986.

When did CADWELL LIMB MOVEMENT MODULE receive FDA 510(k) clearance?

CADWELL LIMB MOVEMENT MODULE received FDA 510(k) clearance on 2004-07-01, under 510(k) number K040986.

Who is the listed applicant for CADWELL LIMB MOVEMENT MODULE?

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

What is the FDA product code for CADWELL LIMB MOVEMENT MODULE?

The FDA product code for CADWELL LIMB MOVEMENT MODULE is LEL.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Cadwell Laboratories, Inc. as applicant

K061706CADWELL EASYNET OXIMETER MODULE K061705CADWELL EASYNET NASAL PRESSURE MODULE K042350TES-1 CONSTANT VOLTAGE ELECTRICAL STIMULATOR K040932EASYNET BODY POSITION MODULE K971214KILOWIN K962455FOUR-CHANNEL PREAMPLIFIER

View all 46 devices →

Related Devices (Code: LEL)

K252981EmbraceMiniEmpatica S.r.l.K251574Sleep WatchAmbulatory Monitoring, Inc.K243513DCM (PW-DCM)Pneumowave, Ltd.K233987VERABAND™Arbor Medical Innovations, LLC K233618Oxevision Sleep DeviceOxehealth Limited K231532ActiGraph LEAP activity monitor (ActiGraph LEAP)Actigraph, LLC

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.