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FDA 510(k)

KODAK EKTASCAN CP PRIMARY HIGH FREQ. VID.INTERFACE

K-Number: K925721 · 1993-02-26

ApplicantEastman Kodak Company
Decision Date1993-02-26
Product CodeLMA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK EKTASCAN CP PRIMARY HIGH FREQ. VID.INTERFACE is the device name listed in this FDA 510(k) record. The listed applicant is Eastman Kodak Company. It received FDA 510(k) clearance on 1993-02-26 under 510(k) number K925721. The device is classified under product code LMA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK EKTASCAN CP PRIMARY HIGH FREQ. VID.INTERFACE?

KODAK EKTASCAN CP PRIMARY HIGH FREQ. VID.INTERFACE is a medical device that received FDA 510(k) clearance on 1993-02-26. The listed applicant is Eastman Kodak Company. The 510(k) number is K925721.

When did KODAK EKTASCAN CP PRIMARY HIGH FREQ. VID.INTERFACE receive FDA 510(k) clearance?

KODAK EKTASCAN CP PRIMARY HIGH FREQ. VID.INTERFACE received FDA 510(k) clearance on 1993-02-26, under 510(k) number K925721.

Who is the listed applicant for KODAK EKTASCAN CP PRIMARY HIGH FREQ. VID.INTERFACE?

The FDA 510(k) record lists Eastman Kodak Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KODAK EKTASCAN CP PRIMARY HIGH FREQ. VID.INTERFACE?

The FDA product code for KODAK EKTASCAN CP PRIMARY HIGH FREQ. VID.INTERFACE is LMA.

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Related Devices (Code: LMA)

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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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