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FDA 510(k)

FUJI MEDICAL CR CONSOLE, MODEL FLASH IIP

K-Number: K041990 · 2004-08-06

ApplicantFujifilm Medical System U.S.A., Inc.
Decision Date2004-08-06
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FUJI MEDICAL CR CONSOLE, MODEL FLASH IIP is the device name listed in this FDA 510(k) record. The listed applicant is Fujifilm Medical System U.S.A., Inc.. It received FDA 510(k) clearance on 2004-08-06 under 510(k) number K041990. 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 FUJI MEDICAL CR CONSOLE, MODEL FLASH IIP?

FUJI MEDICAL CR CONSOLE, MODEL FLASH IIP is a medical device that received FDA 510(k) clearance on 2004-08-06. The listed applicant is Fujifilm Medical System U.S.A., Inc.. The 510(k) number is K041990.

When did FUJI MEDICAL CR CONSOLE, MODEL FLASH IIP receive FDA 510(k) clearance?

FUJI MEDICAL CR CONSOLE, MODEL FLASH IIP received FDA 510(k) clearance on 2004-08-06, under 510(k) number K041990.

Who is the listed applicant for FUJI MEDICAL CR CONSOLE, MODEL FLASH IIP?

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

What is the FDA product code for FUJI MEDICAL CR CONSOLE, MODEL FLASH IIP?

The FDA product code for FUJI MEDICAL CR CONSOLE, MODEL FLASH IIP 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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