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FDA 510(k)

SMART USBLITE, MODEL M011120

K-Number: K061443 · 2006-06-23

ApplicantIntelligent Hearing Systems
Decision Date2006-06-23
Product CodeGWJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SMART USBLITE, MODEL M011120 is the device name listed in this FDA 510(k) record. The listed applicant is Intelligent Hearing Systems. It received FDA 510(k) clearance on 2006-06-23 under 510(k) number K061443. The device is classified under product code GWJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMART USBLITE, MODEL M011120?

SMART USBLITE, MODEL M011120 is a medical device that received FDA 510(k) clearance on 2006-06-23. The listed applicant is Intelligent Hearing Systems. The 510(k) number is K061443.

When did SMART USBLITE, MODEL M011120 receive FDA 510(k) clearance?

SMART USBLITE, MODEL M011120 received FDA 510(k) clearance on 2006-06-23, under 510(k) number K061443.

Who is the listed applicant for SMART USBLITE, MODEL M011120?

The FDA 510(k) record lists Intelligent Hearing Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SMART USBLITE, MODEL M011120?

The FDA product code for SMART USBLITE, MODEL M011120 is GWJ.

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 Intelligent Hearing Systems 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.

K163326SmartEPK090579SMARTSCREENER-PLUS2K073384SMART COUPLER, MODEL M015401K070608SMARTEP, MODEL M010000K063402WICK ELECTRODE, MODEL M019260K052060OPTI-AMP DC-POWERED

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Related Devices (Code: GWJ)

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.

K242954Integrity V500 (Integrity, Integrity with VEMP)Vivosonic, Inc.K233649ALGO Pro Newborn Hearing Screener (ALGO Pro)Natus Medical Incorporated Dba Excel-Tech Ltd. (Xltek)K220139QScreenPath Medical GmbHK211147ALGO 7iPath Medical GmbHK193033GSI Audera ProGrason StadlerK163326SmartEPIntelligent Hearing Systems

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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