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FDA 510(k)

MEDWEB ADVANCED 3D WEB PACS

K-Number: K063221 · 2006-12-12

ApplicantNexsys Electronics, Inc.
Decision Date2006-12-12
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDWEB ADVANCED 3D WEB PACS is the device name listed in this FDA 510(k) record. The listed applicant is Nexsys Electronics, Inc.. It received FDA 510(k) clearance on 2006-12-12 under 510(k) number K063221. 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 MEDWEB ADVANCED 3D WEB PACS?

MEDWEB ADVANCED 3D WEB PACS is a medical device that received FDA 510(k) clearance on 2006-12-12. The listed applicant is Nexsys Electronics, Inc.. The 510(k) number is K063221.

When did MEDWEB ADVANCED 3D WEB PACS receive FDA 510(k) clearance?

MEDWEB ADVANCED 3D WEB PACS received FDA 510(k) clearance on 2006-12-12, under 510(k) number K063221.

Who is the listed applicant for MEDWEB ADVANCED 3D WEB PACS?

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

What is the FDA product code for MEDWEB ADVANCED 3D WEB PACS?

The FDA product code for MEDWEB ADVANCED 3D WEB PACS is LLZ.

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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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