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FDA 510(k)

PACS SOFTWARE SOLUTION 2003

K-Number: K033624 · 2003-12-15

ApplicantCanon USA, Inc.
Decision Date2003-12-15
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PACS SOFTWARE SOLUTION 2003 is the device name listed in this FDA 510(k) record. The listed applicant is Canon USA, Inc.. It received FDA 510(k) clearance on 2003-12-15 under 510(k) number K033624. 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 PACS SOFTWARE SOLUTION 2003?

PACS SOFTWARE SOLUTION 2003 is a medical device that received FDA 510(k) clearance on 2003-12-15. The listed applicant is Canon USA, Inc.. The 510(k) number is K033624.

When did PACS SOFTWARE SOLUTION 2003 receive FDA 510(k) clearance?

PACS SOFTWARE SOLUTION 2003 received FDA 510(k) clearance on 2003-12-15, under 510(k) number K033624.

Who is the listed applicant for PACS SOFTWARE SOLUTION 2003?

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

What is the FDA product code for PACS SOFTWARE SOLUTION 2003?

The FDA product code for PACS SOFTWARE SOLUTION 2003 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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