K-number	K993938
Device name	THE HOMMED SENTRY, MODEL 1 SENTRY
Applicant	Hommed, LLC
Product code	DXN
Device class	Class II
Decision date	Mar 15, 2000
Decision	Substantially Equivalent
Regulation	870.1130

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View the full FDA submission: accessdata.fda.gov

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THE HOMMED SENTRY, MODEL 1 SENTRY

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