K-number	K160240
Device name	Perimeter Otis 1.0 Optical Coherence Tomography System
Applicant	Perimeter Medical Imaging, Inc.
Product code	NQQ
Device class	Class II
Decision date	May 13, 2016
Decision	Unknown
Regulation	892.1560

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View the full FDA submission: accessdata.fda.gov

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Perimeter Otis 1.0 Optical Coherence Tomography System

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Perimeter Otis 1.0 Optical Coherence Tomography System