K-number	K990935
Device name	JACKSON ESOPHAGEAL DILATOR
Applicant	Pilling Weck Surgical
Product code	KNQ
Device class	Class II
Decision date	May 17, 1999
Decision	Substantially Equivalent
Regulation	876.5365

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View the full FDA submission: accessdata.fda.gov

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JACKSON ESOPHAGEAL DILATOR

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