K-number	K791062
Device name	BOUNDARY SPECIALTY GOWN
Applicant	Procter & Gamble Mfg. Co.
Product code	FYA
Device class	Class II
Decision date	Jun 20, 1979
Decision	Substantially Equivalent
Regulation	878.4040

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View the full FDA submission: accessdata.fda.gov

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BOUNDARY SPECIALTY GOWN

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