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FDA 510(k)

KODAK DIGITAL SCIENCE CARDIAC VIEWER

K-Number: K974086 · 1998-01-20

ApplicantEastman Kodak Company
Decision Date1998-01-20
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK DIGITAL SCIENCE CARDIAC VIEWER 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 1998-01-20 under 510(k) number K974086. 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 DIGITAL SCIENCE CARDIAC VIEWER?

KODAK DIGITAL SCIENCE CARDIAC VIEWER is a medical device that received FDA 510(k) clearance on 1998-01-20. The listed applicant is Eastman Kodak Company. The 510(k) number is K974086.

When did KODAK DIGITAL SCIENCE CARDIAC VIEWER receive FDA 510(k) clearance?

KODAK DIGITAL SCIENCE CARDIAC VIEWER received FDA 510(k) clearance on 1998-01-20, under 510(k) number K974086.

Who is the listed applicant for KODAK DIGITAL SCIENCE CARDIAC VIEWER?

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 DIGITAL SCIENCE CARDIAC VIEWER?

The FDA product code for KODAK DIGITAL SCIENCE CARDIAC VIEWER 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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