AIMAGO EASYLDI MICROCIRCULATION CAMERA
K-Number: K121429 · 2012-08-10
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Device Summary
Frequently Asked Questions
What is the AIMAGO EASYLDI MICROCIRCULATION CAMERA?
AIMAGO EASYLDI MICROCIRCULATION CAMERA is a medical device that received FDA 510(k) clearance on 2012-08-10. The listed applicant is Aimago SA. The 510(k) number is K121429.
When did AIMAGO EASYLDI MICROCIRCULATION CAMERA receive FDA 510(k) clearance?
AIMAGO EASYLDI MICROCIRCULATION CAMERA received FDA 510(k) clearance on 2012-08-10, under 510(k) number K121429.
Who is the listed applicant for AIMAGO EASYLDI MICROCIRCULATION CAMERA?
The FDA 510(k) record lists Aimago SA as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AIMAGO EASYLDI MICROCIRCULATION CAMERA?
The FDA product code for AIMAGO EASYLDI MICROCIRCULATION CAMERA is DPT.
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 Aimago SA 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: DPT)
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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