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FDA 510(k)

KODAK EKTASCAN XLP PRELIMINARY DV2000 INTERFACE

K-Number: K912454 · 1991-09-27

ApplicantEastman Kodak Company
Decision Date1991-09-27
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK EKTASCAN XLP PRELIMINARY DV2000 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 1991-09-27 under 510(k) number K912454. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK EKTASCAN XLP PRELIMINARY DV2000 INTERFACE?

KODAK EKTASCAN XLP PRELIMINARY DV2000 INTERFACE is a medical device that received FDA 510(k) clearance on 1991-09-27. The listed applicant is Eastman Kodak Company. The 510(k) number is K912454.

When did KODAK EKTASCAN XLP PRELIMINARY DV2000 INTERFACE receive FDA 510(k) clearance?

KODAK EKTASCAN XLP PRELIMINARY DV2000 INTERFACE received FDA 510(k) clearance on 1991-09-27, under 510(k) number K912454.

Who is the listed applicant for KODAK EKTASCAN XLP PRELIMINARY DV2000 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 XLP PRELIMINARY DV2000 INTERFACE?

The FDA product code for KODAK EKTASCAN XLP PRELIMINARY DV2000 INTERFACE is JAK.

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Other records listing Eastman Kodak Company as applicant

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Related Devices (Code: JAK)

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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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