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FDA 510(k)

KODAK MODELS 2100 AND 2200

K-Number: K060292 · 2006-03-03

ApplicantKodak-Trophy
Decision Date2006-03-03
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KODAK MODELS 2100 AND 2200 is the device name listed in this FDA 510(k) record. The listed applicant is Kodak-Trophy. It received FDA 510(k) clearance on 2006-03-03 under 510(k) number K060292. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK MODELS 2100 AND 2200?

KODAK MODELS 2100 AND 2200 is a medical device that received FDA 510(k) clearance on 2006-03-03. The listed applicant is Kodak-Trophy. The 510(k) number is K060292.

When did KODAK MODELS 2100 AND 2200 receive FDA 510(k) clearance?

KODAK MODELS 2100 AND 2200 received FDA 510(k) clearance on 2006-03-03, under 510(k) number K060292.

Who is the listed applicant for KODAK MODELS 2100 AND 2200?

The FDA 510(k) record lists Kodak-Trophy as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KODAK MODELS 2100 AND 2200?

The FDA product code for KODAK MODELS 2100 AND 2200 is EHD.

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Related Devices (Code: EHD)

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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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