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FDA 510(k)

KODATROL I AND II CONTROL AND DILUENT SET

K-Number: K904768 · 1990-11-09

ApplicantEastman Kodak Company
Decision Date1990-11-09
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KODATROL I AND II CONTROL AND DILUENT SET 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 1990-11-09 under 510(k) number K904768. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODATROL I AND II CONTROL AND DILUENT SET?

KODATROL I AND II CONTROL AND DILUENT SET is a medical device that received FDA 510(k) clearance on 1990-11-09. The listed applicant is Eastman Kodak Company. The 510(k) number is K904768.

When did KODATROL I AND II CONTROL AND DILUENT SET receive FDA 510(k) clearance?

KODATROL I AND II CONTROL AND DILUENT SET received FDA 510(k) clearance on 1990-11-09, under 510(k) number K904768.

Who is the listed applicant for KODATROL I AND II CONTROL AND DILUENT SET?

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 KODATROL I AND II CONTROL AND DILUENT SET?

The FDA product code for KODATROL I AND II CONTROL AND DILUENT SET is JJY.

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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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