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FDA 510(k)

KODAK EKTACHEM DT SLIDES (LAC)

K-Number: K913197 · 1991-08-26

Decision Date1991-08-26
Product CodeKHP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KODAK EKTACHEM DT SLIDES (LAC) 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 1991-08-26 under 510(k) number K913197. The device is classified under product code KHP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK EKTACHEM DT SLIDES (LAC)?

KODAK EKTACHEM DT SLIDES (LAC) is a medical device that received FDA 510(k) clearance on 1991-08-26. The listed applicant is Eastman Kodak Company. The 510(k) number is K913197.

When did KODAK EKTACHEM DT SLIDES (LAC) receive FDA 510(k) clearance?

KODAK EKTACHEM DT SLIDES (LAC) received FDA 510(k) clearance on 1991-08-26, under 510(k) number K913197.

Who is the listed applicant for KODAK EKTACHEM DT SLIDES (LAC)?

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 EKTACHEM DT SLIDES (LAC)?

The FDA product code for KODAK EKTACHEM DT SLIDES (LAC) is KHP.

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: KHP)

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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