TUBING CONNECTORS EC-2XXX SERIES (K833322) — FDA 510(k) Clearance | Predicase

K-number	K833322
Device name	TUBING CONNECTORS EC-2XXX SERIES
Applicant	Gish Biomedical, Inc.
Product code	DTL
Device class	Class II
Decision date	Dec 16, 1983
Decision	Substantially Equivalent
Regulation	870.4290

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View the full FDA submission: accessdata.fda.gov

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