K-number	K896120
Device name	SCHILLER MODEL SP-100 SPIROVIT(TM)
Applicant	Schiller America, Inc.
Product code	BZG
Device class	Class II
Decision date	Jan 9, 1990
Decision	Substantially Equivalent
Regulation	868.1840

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View the full FDA submission: accessdata.fda.gov

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SCHILLER MODEL SP-100 SPIROVIT(TM)

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