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FDA 510(k)

FUJI MEDICAL LASER IMAGERMULTI-FORMATTERS MF-300 AND MF-300L

K-Number: K950721 · 1995-05-24

ApplicantFujifilm Medical System U.S.A., Inc.
Decision Date1995-05-24
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FUJI MEDICAL LASER IMAGERMULTI-FORMATTERS MF-300 AND MF-300L 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 1995-05-24 under 510(k) number K950721. The device is classified under product code LMC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUJI MEDICAL LASER IMAGERMULTI-FORMATTERS MF-300 AND MF-300L?

FUJI MEDICAL LASER IMAGERMULTI-FORMATTERS MF-300 AND MF-300L is a medical device that received FDA 510(k) clearance on 1995-05-24. The listed applicant is Fujifilm Medical System U.S.A., Inc.. The 510(k) number is K950721.

When did FUJI MEDICAL LASER IMAGERMULTI-FORMATTERS MF-300 AND MF-300L receive FDA 510(k) clearance?

FUJI MEDICAL LASER IMAGERMULTI-FORMATTERS MF-300 AND MF-300L received FDA 510(k) clearance on 1995-05-24, under 510(k) number K950721.

Who is the listed applicant for FUJI MEDICAL LASER IMAGERMULTI-FORMATTERS MF-300 AND MF-300L?

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 IMAGERMULTI-FORMATTERS MF-300 AND MF-300L?

The FDA product code for FUJI MEDICAL LASER IMAGERMULTI-FORMATTERS MF-300 AND MF-300L is LMC.

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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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