K-number	K840342
Device name	PDI PREPMASTER WET PACK PATIENT PREP KIT
Applicant	Nice-Pak Products, Inc.
Product code	FRG
Device class	Class II
Decision date	Mar 27, 1984
Decision	Substantially Equivalent
Regulation	880.6850

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View the full FDA submission: accessdata.fda.gov

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PDI PREPMASTER WET PACK PATIENT PREP KIT

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