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FDA 510(k)

KODAK AUTOMIXER III INTEGRATED, KODAK AUTOMIXER III 180 LP

K-Number: K940386 · 1994-08-17

ApplicantEastman Kodak Company
Decision Date1994-08-17
Product CodeIXL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK AUTOMIXER III INTEGRATED, KODAK AUTOMIXER III 180 LP 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 1994-08-17 under 510(k) number K940386. The device is classified under product code IXL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK AUTOMIXER III INTEGRATED, KODAK AUTOMIXER III 180 LP?

KODAK AUTOMIXER III INTEGRATED, KODAK AUTOMIXER III 180 LP is a medical device that received FDA 510(k) clearance on 1994-08-17. The listed applicant is Eastman Kodak Company. The 510(k) number is K940386.

When did KODAK AUTOMIXER III INTEGRATED, KODAK AUTOMIXER III 180 LP receive FDA 510(k) clearance?

KODAK AUTOMIXER III INTEGRATED, KODAK AUTOMIXER III 180 LP received FDA 510(k) clearance on 1994-08-17, under 510(k) number K940386.

Who is the listed applicant for KODAK AUTOMIXER III INTEGRATED, KODAK AUTOMIXER III 180 LP?

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 AUTOMIXER III INTEGRATED, KODAK AUTOMIXER III 180 LP?

The FDA product code for KODAK AUTOMIXER III INTEGRATED, KODAK AUTOMIXER III 180 LP is IXL.

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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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