TRELLIS INFUSION SYSTEM (10CM INFUSION LENGTH); TRELLIS INFUSION SYSTEM (20CM INFUSION LENGTH)— 510(k) K013635

Substantially Equivalent

Bacchus Vascular, Inc.

FDA 510(k) clearance K013635 for TRELLIS INFUSION SYSTEM (10CM INFUSION LENGTH); TRELLIS INFUSION SYSTEM (20CM INFUSION LENGTH), Substantially Equivalent on 2002-02-11. Applicant: Bacchus Vascular, Inc.. Device class: 2.

Clearance details

Applicant
Bacchus Vascular, Inc.
Product code
Code QEY
Device class
Class 2
Regulation
21 CFR 870.5150
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Santa Clara, CA, US
Download summary PDFView on FDA.gov ↗

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