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FDA 510(k)

KODAK DRYVIEW 8900 LASER IMAGER MAMMOGRAPHY ACCESSORY

K-Number: K033821 · 2004-02-20

ApplicantEastman Kodak Company
Decision Date2004-02-20
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK DRYVIEW 8900 LASER IMAGER MAMMOGRAPHY ACCESSORY 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 2004-02-20 under 510(k) number K033821. The device is classified under product code LMC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK DRYVIEW 8900 LASER IMAGER MAMMOGRAPHY ACCESSORY?

KODAK DRYVIEW 8900 LASER IMAGER MAMMOGRAPHY ACCESSORY is a medical device that received FDA 510(k) clearance on 2004-02-20. The listed applicant is Eastman Kodak Company. The 510(k) number is K033821.

When did KODAK DRYVIEW 8900 LASER IMAGER MAMMOGRAPHY ACCESSORY receive FDA 510(k) clearance?

KODAK DRYVIEW 8900 LASER IMAGER MAMMOGRAPHY ACCESSORY received FDA 510(k) clearance on 2004-02-20, under 510(k) number K033821.

Who is the listed applicant for KODAK DRYVIEW 8900 LASER IMAGER MAMMOGRAPHY ACCESSORY?

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 DRYVIEW 8900 LASER IMAGER MAMMOGRAPHY ACCESSORY?

The FDA product code for KODAK DRYVIEW 8900 LASER IMAGER MAMMOGRAPHY ACCESSORY is LMC.

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Related Devices (Code: LMC)

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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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