K-number	K831357
Device name	BOUNDARY HEADWEAR
Applicant	Procter & Gamble Mfg. Co.
Product code	FYF
Device class	Class I
Decision date	Jun 2, 1983
Decision	Substantially Equivalent
Regulation	878.4040

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View the full FDA submission: accessdata.fda.gov

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BOUNDARY HEADWEAR

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