Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SENSOR WALK

K-Number: K052771 · 2006-05-03

ApplicantOtto Bock Healthcare LP
Decision Date2006-05-03
Product CodeIQI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SENSOR WALK is the device name listed in this FDA 510(k) record. The listed applicant is Otto Bock Healthcare LP. It received FDA 510(k) clearance on 2006-05-03 under 510(k) number K052771. The device is classified under product code IQI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENSOR WALK?

SENSOR WALK is a medical device that received FDA 510(k) clearance on 2006-05-03. The listed applicant is Otto Bock Healthcare LP. The 510(k) number is K052771.

When did SENSOR WALK receive FDA 510(k) clearance?

SENSOR WALK received FDA 510(k) clearance on 2006-05-03, under 510(k) number K052771.

Who is the listed applicant for SENSOR WALK?

The FDA 510(k) record lists Otto Bock Healthcare LP as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SENSOR WALK?

The FDA product code for SENSOR WALK is IQI.

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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Otto Bock Healthcare LP 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.

K213587MyCRO BandK201426MyCRO BandK113164DISCOVERY TMAX MANUAL WHEELCHAIRK111278Z10 WHEELCHAIR PUSH AND BRAKE ASSIST DEVICEK111045CENTRO FAMILY OF MANUAL WHEELCHAIRSK101524C2000 POWERED WHEELCHAIR

View all 17 devices →

Related Devices (Code: IQI)

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.

K031576SPARTAN ORTHOPAEDIC WRIST BRACE, MODEL SCT-1Surgitech, Inc.K926391ACCUFLEX DYNAMIC ELBOW ORTHOSISRegulatory & Marketing Services, Inc.K910974MCCONNELL SHOULDER BRACEMcconnell OrthopedicK874502GAIT-AID ORTHOPEDIC INSOLEGait-Aid, Inc.K831542ADJUSTABLE POLYCENTRIC ELBOW HINGEFred Sammons, Inc.K831615DROP FOOT BRACEEdward Dilauro, Jr.

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.

↑