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FDA 510(k)

KODAK X-OMAT MULTILOADER 300

K-Number: K905607 · 1991-03-12

Decision Date1991-03-12
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK X-OMAT MULTILOADER 300 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 1991-03-12 under 510(k) number K905607. The device is classified under product code IXW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK X-OMAT MULTILOADER 300?

KODAK X-OMAT MULTILOADER 300 is a medical device that received FDA 510(k) clearance on 1991-03-12. The listed applicant is Eastman Kodak Company. The 510(k) number is K905607.

When did KODAK X-OMAT MULTILOADER 300 receive FDA 510(k) clearance?

KODAK X-OMAT MULTILOADER 300 received FDA 510(k) clearance on 1991-03-12, under 510(k) number K905607.

Who is the listed applicant for KODAK X-OMAT MULTILOADER 300?

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 X-OMAT MULTILOADER 300?

The FDA product code for KODAK X-OMAT MULTILOADER 300 is IXW.

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.

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Related Devices (Code: IXW)

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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