K-number	K151696
Device name	Caiman Seal and Cut Technology
Applicant	Aesculap, Inc.
Product code	GEI
Device class	Class II
Decision date	Jul 20, 2015
Decision	Substantially Equivalent
Regulation	878.4400

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Source

View the full FDA submission: accessdata.fda.gov

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Caiman Seal and Cut Technology

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