K-number	K820670
Device name	HS17/HS18 SERIES MONITORS
Applicant	Medtel Pty. , Ltd.
Product code	FLL
Device class	Class II
Decision date	Apr 9, 1982
Decision	Substantially Equivalent
Regulation	880.2910

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View the full FDA submission: accessdata.fda.gov

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HS17/HS18 SERIES MONITORS

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