NICOM DIGITAL IMAGE MANAGER
K-Number: K945654 · 1995-02-17
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Device Summary
Frequently Asked Questions
What is the NICOM DIGITAL IMAGE MANAGER?
NICOM DIGITAL IMAGE MANAGER is a medical device that received FDA 510(k) clearance on 1995-02-17. The listed applicant is Camtronics, Ltd.. The 510(k) number is K945654.
When did NICOM DIGITAL IMAGE MANAGER receive FDA 510(k) clearance?
NICOM DIGITAL IMAGE MANAGER received FDA 510(k) clearance on 1995-02-17, under 510(k) number K945654.
Who is the listed applicant for NICOM DIGITAL IMAGE MANAGER?
The FDA 510(k) record lists Camtronics, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NICOM DIGITAL IMAGE MANAGER?
The FDA product code for NICOM DIGITAL IMAGE MANAGER is LMB.
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 Camtronics, Ltd. 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: LMB)
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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