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FDA 510(k)

FUJI IP CASSETTE TYPE PC

K-Number: K070920 · 2007-05-22

ApplicantFujifilm Medical Systems U.S.A, Inc.
Decision Date2007-05-22
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FUJI IP CASSETTE TYPE PC 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 2007-05-22 under 510(k) number K070920. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUJI IP CASSETTE TYPE PC?

FUJI IP CASSETTE TYPE PC is a medical device that received FDA 510(k) clearance on 2007-05-22. The listed applicant is Fujifilm Medical Systems U.S.A, Inc.. The 510(k) number is K070920.

When did FUJI IP CASSETTE TYPE PC receive FDA 510(k) clearance?

FUJI IP CASSETTE TYPE PC received FDA 510(k) clearance on 2007-05-22, under 510(k) number K070920.

Who is the listed applicant for FUJI IP CASSETTE TYPE PC?

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 FUJI IP CASSETTE TYPE PC?

The FDA product code for FUJI IP CASSETTE TYPE PC is IYE.

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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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