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FDA 510(k)

KODAK EKTASCAN IMAGE TRANSMISSION SYSTEM

K-Number: K855002 · 1986-04-07

ApplicantEastman Kodak Company
Decision Date1986-04-07
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK EKTASCAN IMAGE TRANSMISSION SYSTEM 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 1986-04-07 under 510(k) number K855002. 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 KODAK EKTASCAN IMAGE TRANSMISSION SYSTEM?

KODAK EKTASCAN IMAGE TRANSMISSION SYSTEM is a medical device that received FDA 510(k) clearance on 1986-04-07. The listed applicant is Eastman Kodak Company. The 510(k) number is K855002.

When did KODAK EKTASCAN IMAGE TRANSMISSION SYSTEM receive FDA 510(k) clearance?

KODAK EKTASCAN IMAGE TRANSMISSION SYSTEM received FDA 510(k) clearance on 1986-04-07, under 510(k) number K855002.

Who is the listed applicant for KODAK EKTASCAN IMAGE TRANSMISSION SYSTEM?

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 IMAGE TRANSMISSION SYSTEM?

The FDA product code for KODAK EKTASCAN IMAGE TRANSMISSION SYSTEM is LLZ.

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Other records listing Eastman Kodak Company as applicant

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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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