K-number	K921798
Device name	PROPPER SUPER SERACULT(R)
Applicant	Propper Mfg. Co., Inc.
Product code	KHE
Device class	Class II
Decision date	Oct 5, 1992
Decision	Substantially Equivalent
Regulation	864.6550

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View the full FDA submission: accessdata.fda.gov

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PROPPER SUPER SERACULT(R)

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