K-number	K000572
Device name	E.N.S.I. SYRINGE
Applicant	Tri-Ject Intl. Corp.
Product code	MEG
Device class	Class II
Decision date	Feb 24, 2000
Decision	Substantially Equivalent
Regulation	880.5860

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View the full FDA submission: accessdata.fda.gov

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E.N.S.I. SYRINGE

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