KODAK DIGITAL SCIENCE MEDICAL PRINTER INTERFACE UNIT
K-Number: K961740 · 1996-11-14
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Device Summary
Frequently Asked Questions
What is the KODAK DIGITAL SCIENCE MEDICAL PRINTER INTERFACE UNIT?
KODAK DIGITAL SCIENCE MEDICAL PRINTER INTERFACE UNIT is a medical device that received FDA 510(k) clearance on 1996-11-14. The listed applicant is Kodak Health Imaging Systems, Inc.. The 510(k) number is K961740.
When did KODAK DIGITAL SCIENCE MEDICAL PRINTER INTERFACE UNIT receive FDA 510(k) clearance?
KODAK DIGITAL SCIENCE MEDICAL PRINTER INTERFACE UNIT received FDA 510(k) clearance on 1996-11-14, under 510(k) number K961740.
Who is the listed applicant for KODAK DIGITAL SCIENCE MEDICAL PRINTER INTERFACE UNIT?
The FDA 510(k) record lists Kodak Health Imaging Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KODAK DIGITAL SCIENCE MEDICAL PRINTER INTERFACE UNIT?
The FDA product code for KODAK DIGITAL SCIENCE MEDICAL PRINTER INTERFACE UNIT is LLZ.
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 Kodak Health Imaging Systems, Inc. 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: LLZ)
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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