DIGITAL IMAGE ENHANCEMENT SYSTEM
K-Number: K900851 · 1990-05-11
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Device Summary
Frequently Asked Questions
What is the DIGITAL IMAGE ENHANCEMENT SYSTEM?
DIGITAL IMAGE ENHANCEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1990-05-11. The listed applicant is Atomic Products Corp.. The 510(k) number is K900851.
When did DIGITAL IMAGE ENHANCEMENT SYSTEM receive FDA 510(k) clearance?
DIGITAL IMAGE ENHANCEMENT SYSTEM received FDA 510(k) clearance on 1990-05-11, under 510(k) number K900851.
Who is the listed applicant for DIGITAL IMAGE ENHANCEMENT SYSTEM?
The FDA 510(k) record lists Atomic Products Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIGITAL IMAGE ENHANCEMENT SYSTEM?
The FDA product code for DIGITAL IMAGE ENHANCEMENT SYSTEM 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 Atomic Products Corp. 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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