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FDA 510(k)

FUJI MEDICAL LASER IMAGER MF PRINT SERVER MF-PS667

K-Number: K970349 · 1997-03-31

ApplicantFujifilm Medical System U.S.A., Inc.
Decision Date1997-03-31
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FUJI MEDICAL LASER IMAGER MF PRINT SERVER MF-PS667 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 1997-03-31 under 510(k) number K970349. 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 LASER IMAGER MF PRINT SERVER MF-PS667?

FUJI MEDICAL LASER IMAGER MF PRINT SERVER MF-PS667 is a medical device that received FDA 510(k) clearance on 1997-03-31. The listed applicant is Fujifilm Medical System U.S.A., Inc.. The 510(k) number is K970349.

When did FUJI MEDICAL LASER IMAGER MF PRINT SERVER MF-PS667 receive FDA 510(k) clearance?

FUJI MEDICAL LASER IMAGER MF PRINT SERVER MF-PS667 received FDA 510(k) clearance on 1997-03-31, under 510(k) number K970349.

Who is the listed applicant for FUJI MEDICAL LASER IMAGER MF PRINT SERVER MF-PS667?

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 LASER IMAGER MF PRINT SERVER MF-PS667?

The FDA product code for FUJI MEDICAL LASER IMAGER MF PRINT SERVER MF-PS667 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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