OTIS Optical Coherence Tomography System
K-Number: K171560 · 2017-08-25
Device Summary
Frequently Asked Questions
What is the OTIS Optical Coherence Tomography System?
OTIS Optical Coherence Tomography System is a medical device that received FDA 510(k) clearance on 2017-08-25. It is manufactured by Perimeter Medical Imaging, Inc.. The 510(k) number is K171560.
When was OTIS Optical Coherence Tomography System approved by the FDA?
OTIS Optical Coherence Tomography System received FDA 510(k) clearance on 2017-08-25, under approval number K171560.
What company makes OTIS Optical Coherence Tomography System?
OTIS Optical Coherence Tomography System is manufactured by Perimeter Medical Imaging, Inc..
What is the FDA product code for OTIS Optical Coherence Tomography System?
The FDA product code for OTIS Optical Coherence Tomography System is NQQ.
Related Clinical Trials
Other Devices by Perimeter Medical Imaging, Inc.
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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.