SEEMOR 5.0 IMAGE DISPLAY PROGRAM
K-Number: K041782 · 2004-08-16
Advertisement
Device Summary
Frequently Asked Questions
What is the SEEMOR 5.0 IMAGE DISPLAY PROGRAM?
SEEMOR 5.0 IMAGE DISPLAY PROGRAM is a medical device that received FDA 510(k) clearance on 2004-08-16. The listed applicant is Areeda Assoc., Ltd.. The 510(k) number is K041782.
When did SEEMOR 5.0 IMAGE DISPLAY PROGRAM receive FDA 510(k) clearance?
SEEMOR 5.0 IMAGE DISPLAY PROGRAM received FDA 510(k) clearance on 2004-08-16, under 510(k) number K041782.
Who is the listed applicant for SEEMOR 5.0 IMAGE DISPLAY PROGRAM?
The FDA 510(k) record lists Areeda Assoc., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SEEMOR 5.0 IMAGE DISPLAY PROGRAM?
The FDA product code for SEEMOR 5.0 IMAGE DISPLAY PROGRAM 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 Areeda Assoc., 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: 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.
Advertisement