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FDA 510(k)

SYNAPSE MIP/MPR IMAGE VISUALIZATION SOFTWARE OBLIQUUS

K-Number: K061672 · 2006-06-29

ApplicantFujifilm Medical Systems U.S.A, Inc.
Decision Date2006-06-29
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SYNAPSE MIP/MPR IMAGE VISUALIZATION SOFTWARE OBLIQUUS is the device name listed in this FDA 510(k) record. The listed applicant is Fujifilm Medical Systems U.S.A, Inc.. It received FDA 510(k) clearance on 2006-06-29 under 510(k) number K061672. 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 SYNAPSE MIP/MPR IMAGE VISUALIZATION SOFTWARE OBLIQUUS?

SYNAPSE MIP/MPR IMAGE VISUALIZATION SOFTWARE OBLIQUUS is a medical device that received FDA 510(k) clearance on 2006-06-29. The listed applicant is Fujifilm Medical Systems U.S.A, Inc.. The 510(k) number is K061672.

When did SYNAPSE MIP/MPR IMAGE VISUALIZATION SOFTWARE OBLIQUUS receive FDA 510(k) clearance?

SYNAPSE MIP/MPR IMAGE VISUALIZATION SOFTWARE OBLIQUUS received FDA 510(k) clearance on 2006-06-29, under 510(k) number K061672.

Who is the listed applicant for SYNAPSE MIP/MPR IMAGE VISUALIZATION SOFTWARE OBLIQUUS?

The FDA 510(k) record lists Fujifilm Medical Systems U.S.A, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYNAPSE MIP/MPR IMAGE VISUALIZATION SOFTWARE OBLIQUUS?

The FDA product code for SYNAPSE MIP/MPR IMAGE VISUALIZATION SOFTWARE OBLIQUUS 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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