KODAK X-OMAT M20 PROCESSOR, MODEL 1
K-Number: K792435 · 1980-01-09
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Device Summary
Frequently Asked Questions
What is the KODAK X-OMAT M20 PROCESSOR, MODEL 1?
KODAK X-OMAT M20 PROCESSOR, MODEL 1 is a medical device that received FDA 510(k) clearance on 1980-01-09. The listed applicant is Eastman Kodak Company. The 510(k) number is K792435.
When did KODAK X-OMAT M20 PROCESSOR, MODEL 1 receive FDA 510(k) clearance?
KODAK X-OMAT M20 PROCESSOR, MODEL 1 received FDA 510(k) clearance on 1980-01-09, under 510(k) number K792435.
Who is the listed applicant for KODAK X-OMAT M20 PROCESSOR, MODEL 1?
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 M20 PROCESSOR, MODEL 1?
The FDA product code for KODAK X-OMAT M20 PROCESSOR, MODEL 1 is IWZ.
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.
Related Devices (Code: IWZ)
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
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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