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FDA 510(k)

SONOVIEW PRO BY MEDISON CO., LTD.

K-Number: K031886 · 2003-06-30

ApplicantMedison Co., Ltd.
Decision Date2003-06-30
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SONOVIEW PRO BY MEDISON CO., LTD. is the device name listed in this FDA 510(k) record. The listed applicant is Medison Co., Ltd.. It received FDA 510(k) clearance on 2003-06-30 under 510(k) number K031886. 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 SONOVIEW PRO BY MEDISON CO., LTD.?

SONOVIEW PRO BY MEDISON CO., LTD. is a medical device that received FDA 510(k) clearance on 2003-06-30. The listed applicant is Medison Co., Ltd.. The 510(k) number is K031886.

When did SONOVIEW PRO BY MEDISON CO., LTD. receive FDA 510(k) clearance?

SONOVIEW PRO BY MEDISON CO., LTD. received FDA 510(k) clearance on 2003-06-30, under 510(k) number K031886.

Who is the listed applicant for SONOVIEW PRO BY MEDISON CO., LTD.?

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

What is the FDA product code for SONOVIEW PRO BY MEDISON CO., LTD.?

The FDA product code for SONOVIEW PRO BY MEDISON CO., LTD. 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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