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FDA 510(k)

KODAK DIGITAL SCIENCE-DENTAL IMAGE VIEWER

K-Number: K973476 · 1997-11-10

Decision Date1997-11-10
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KODAK DIGITAL SCIENCE-DENTAL IMAGE 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 1997-11-10 under 510(k) number K973476. 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 DIGITAL SCIENCE-DENTAL IMAGE VIEWER?

KODAK DIGITAL SCIENCE-DENTAL IMAGE VIEWER is a medical device that received FDA 510(k) clearance on 1997-11-10. The listed applicant is Eastman Kodak Company. The 510(k) number is K973476.

When did KODAK DIGITAL SCIENCE-DENTAL IMAGE VIEWER receive FDA 510(k) clearance?

KODAK DIGITAL SCIENCE-DENTAL IMAGE VIEWER received FDA 510(k) clearance on 1997-11-10, under 510(k) number K973476.

Who is the listed applicant for KODAK DIGITAL SCIENCE-DENTAL IMAGE 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-DENTAL IMAGE VIEWER?

The FDA product code for KODAK DIGITAL SCIENCE-DENTAL IMAGE VIEWER is EHD.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Eastman Kodak Company as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 238 devices →

Related Devices (Code: EHD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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