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FDA 510(k)

VIEWSEND MEDICAL SYSTEM

K-Number: K051586 · 2005-08-04

ApplicantKenei Co., Ltd.
Decision Date2005-08-04
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIEWSEND MEDICAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Kenei Co., Ltd.. It received FDA 510(k) clearance on 2005-08-04 under 510(k) number K051586. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIEWSEND MEDICAL SYSTEM?

VIEWSEND MEDICAL SYSTEM is a medical device that received FDA 510(k) clearance on 2005-08-04. The listed applicant is Kenei Co., Ltd.. The 510(k) number is K051586.

When did VIEWSEND MEDICAL SYSTEM receive FDA 510(k) clearance?

VIEWSEND MEDICAL SYSTEM received FDA 510(k) clearance on 2005-08-04, under 510(k) number K051586.

Who is the listed applicant for VIEWSEND MEDICAL SYSTEM?

The FDA 510(k) record lists Kenei Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIEWSEND MEDICAL SYSTEM?

The FDA product code for VIEWSEND MEDICAL SYSTEM is LLZ.

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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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