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FDA 510(k)

KODAK EKTASCAN IMAGE TRANS SYS T1/R1 SOFTWARE,1.10

K-Number: K864927 · 1987-02-11

ApplicantEastman Kodak Company
Decision Date1987-02-11
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK EKTASCAN IMAGE TRANS SYS T1/R1 SOFTWARE,1.10 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 1987-02-11 under 510(k) number K864927. 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 TRANS SYS T1/R1 SOFTWARE,1.10?

KODAK EKTASCAN IMAGE TRANS SYS T1/R1 SOFTWARE,1.10 is a medical device that received FDA 510(k) clearance on 1987-02-11. The listed applicant is Eastman Kodak Company. The 510(k) number is K864927.

When did KODAK EKTASCAN IMAGE TRANS SYS T1/R1 SOFTWARE,1.10 receive FDA 510(k) clearance?

KODAK EKTASCAN IMAGE TRANS SYS T1/R1 SOFTWARE,1.10 received FDA 510(k) clearance on 1987-02-11, under 510(k) number K864927.

Who is the listed applicant for KODAK EKTASCAN IMAGE TRANS SYS T1/R1 SOFTWARE,1.10?

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 TRANS SYS T1/R1 SOFTWARE,1.10?

The FDA product code for KODAK EKTASCAN IMAGE TRANS SYS T1/R1 SOFTWARE,1.10 is LLZ.

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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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