K-number	K944244
Device name	MODEL E278OR-ASP SERIES RETRACTABLE
Applicant	Valleylab, Inc.
Product code	GEI
Device class	Class II
Decision date	Nov 30, 1994
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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MODEL E278OR-ASP SERIES RETRACTABLE

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