VECTOR AMBULATORY DRUG DELIVERY SYSTEM— 510(k) K935461

Name: FDA 510(k) clearance K935461
Creator: U.S. Food and Drug Administration
Published: 1994-04-28

Substantially Equivalent

Infusion Technology Intl.

FDA 510(k) clearance K935461 for VECTOR AMBULATORY DRUG DELIVERY SYSTEM, Substantially Equivalent on 1994-04-28. Applicant: Infusion Technology Intl.. Device class: 2.

Clearance details

Applicant: Infusion Technology Intl.
Product code: Code FIH
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 1993-11-12
Decision date: 1994-04-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Danvers, MA, US

Download summary PDF View on FDA.gov ↗

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K932055 — PERCUPUMP II1995-03-21
K931113 — CADD-TPN(TM) AMBULATORY INFUSION SYSTEM1994-04-28
K900439 — SINGLE-USE, STERILE, PREFILLED SYRINGE, 60CC1990-02-15
K881707 — INTROCULAR FLUID INJECTOR1988-10-21

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K943591 — VECTOR(TM) AMBULATORY DRUG DELIVERY SYSTEM1995-06-28
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