K-number	K062413
Device name	AESCULAP PNEUMATIC KERRISON
Applicant	Aesculap, Inc.
Product code	HAD
Device class	Class II
Decision date	Nov 21, 2006
Decision	Substantially Equivalent
Regulation	882.4845

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Source

View the full FDA submission: accessdata.fda.gov

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AESCULAP PNEUMATIC KERRISON

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