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FDA 510(k)

EZ-SCOPE AN & EZ-SCOPE AN LITE

K-Number: K020643 · 2002-05-28

ApplicantHealth Policy Resorters Group, LLC
Decision Date2002-05-28
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

EZ-SCOPE AN & EZ-SCOPE AN LITE is the device name listed in this FDA 510(k) record. The listed applicant is Health Policy Resorters Group, LLC. It received FDA 510(k) clearance on 2002-05-28 under 510(k) number K020643. The device is classified under product code IYX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZ-SCOPE AN & EZ-SCOPE AN LITE?

EZ-SCOPE AN & EZ-SCOPE AN LITE is a medical device that received FDA 510(k) clearance on 2002-05-28. The listed applicant is Health Policy Resorters Group, LLC. The 510(k) number is K020643.

When did EZ-SCOPE AN & EZ-SCOPE AN LITE receive FDA 510(k) clearance?

EZ-SCOPE AN & EZ-SCOPE AN LITE received FDA 510(k) clearance on 2002-05-28, under 510(k) number K020643.

Who is the listed applicant for EZ-SCOPE AN & EZ-SCOPE AN LITE?

The FDA 510(k) record lists Health Policy Resorters Group, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EZ-SCOPE AN & EZ-SCOPE AN LITE?

The FDA product code for EZ-SCOPE AN & EZ-SCOPE AN LITE is IYX.

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Related Devices (Code: IYX)

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.

K230221QDOSE® Multi-purpose Voxel Dosimetry (Personalized Dosimetry in Molecular Radiotherapy)Versant Medical Physics and Radiation SafetyK2125873D-RD-SRadiopharmaceutical Imaging and Dosimetry, LLCK163687OLINDA EXMHermes Medical Solutions ABK160933Discovery NM 750b BopsyGE HealthcareK162052Sentinella 102, Sentinella 102 HorusGeneral Equipment For Medical Imaging (Oncovision-K123408ERGO IMAGING SYSTEMDigirad 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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