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FDA 510(k)

DVNET MDV-PACS

K-Number: K031816 · 2003-08-14

ApplicantDvnet International Technology Co., Ltd.
Decision Date2003-08-14
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DVNET MDV-PACS is the device name listed in this FDA 510(k) record. The listed applicant is Dvnet International Technology Co., Ltd.. It received FDA 510(k) clearance on 2003-08-14 under 510(k) number K031816. 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 DVNET MDV-PACS?

DVNET MDV-PACS is a medical device that received FDA 510(k) clearance on 2003-08-14. The listed applicant is Dvnet International Technology Co., Ltd.. The 510(k) number is K031816.

When did DVNET MDV-PACS receive FDA 510(k) clearance?

DVNET MDV-PACS received FDA 510(k) clearance on 2003-08-14, under 510(k) number K031816.

Who is the listed applicant for DVNET MDV-PACS?

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

What is the FDA product code for DVNET MDV-PACS?

The FDA product code for DVNET MDV-PACS is LLZ.

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Related Devices (Code: LLZ)

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.

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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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