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FDA 510(k)

WHS-1000 WOUND HEALING SYSTEM

K-Number: K050156 · 2005-06-17

ApplicantIyia Technologies, Inc.
Decision Date2005-06-17
Product CodeKPJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WHS-1000 WOUND HEALING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Iyia Technologies, Inc.. It received FDA 510(k) clearance on 2005-06-17 under 510(k) number K050156. The device is classified under product code KPJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHS-1000 WOUND HEALING SYSTEM?

WHS-1000 WOUND HEALING SYSTEM is a medical device that received FDA 510(k) clearance on 2005-06-17. The listed applicant is Iyia Technologies, Inc.. The 510(k) number is K050156.

When did WHS-1000 WOUND HEALING SYSTEM receive FDA 510(k) clearance?

WHS-1000 WOUND HEALING SYSTEM received FDA 510(k) clearance on 2005-06-17, under 510(k) number K050156.

Who is the listed applicant for WHS-1000 WOUND HEALING SYSTEM?

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

What is the FDA product code for WHS-1000 WOUND HEALING SYSTEM?

The FDA product code for WHS-1000 WOUND HEALING SYSTEM is KPJ.

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Related Devices (Code: KPJ)

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.

K250188Wound Treatment System (VHT-200)Vaporox, Inc.K212121VHT-200 Wound Treatment SystemVaporox, Inc.K190742EPIFLO-28Neogenix, LLC Dba OgenixK112634NATROX TOPICAL OXYGEN DELIVERY SYSTEM WITH IODPInotec Amd , Ltd.K120764EPIFLO(R)Neogenix, LLCK090681TANSCU O2Electrochemical Oxygen Concepts, Inc.

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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