K-number	K014149
Device name	PAEDISCOPE, MODEL # P010A AND PF011A
Applicant	Aesculap, Inc.
Product code	GWG
Device class	Class II
Decision date	Mar 18, 2002
Decision	Substantially Equivalent
Regulation	882.1480

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View the full FDA submission: accessdata.fda.gov

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PAEDISCOPE, MODEL # P010A AND PF011A

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