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FDA 510(k)

FUJI MEDICAL DRY IMAGER FM-DP 2636

K-Number: K962967 · 1996-10-28

ApplicantFujifilm Medical System U.S.A., Inc.
Decision Date1996-10-28
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FUJI MEDICAL DRY IMAGER FM-DP 2636 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 1996-10-28 under 510(k) number K962967. 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 DRY IMAGER FM-DP 2636?

FUJI MEDICAL DRY IMAGER FM-DP 2636 is a medical device that received FDA 510(k) clearance on 1996-10-28. The listed applicant is Fujifilm Medical System U.S.A., Inc.. The 510(k) number is K962967.

When did FUJI MEDICAL DRY IMAGER FM-DP 2636 receive FDA 510(k) clearance?

FUJI MEDICAL DRY IMAGER FM-DP 2636 received FDA 510(k) clearance on 1996-10-28, under 510(k) number K962967.

Who is the listed applicant for FUJI MEDICAL DRY IMAGER FM-DP 2636?

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 DRY IMAGER FM-DP 2636?

The FDA product code for FUJI MEDICAL DRY IMAGER FM-DP 2636 is LMC.

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Other records listing Fujifilm Medical System U.S.A., Inc. as applicant

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Related Devices (Code: 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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