K-number	K920210
Device name	SRH-678 VACCUUM TUBING
Applicant	Quinn Healthcare Products
Product code	FYD
Device class	Class II
Decision date	Oct 1, 1992
Decision	Substantially Equivalent
Regulation	878.5070

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View the full FDA submission: accessdata.fda.gov

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SRH-678 VACCUUM TUBING

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