EXEL INDWELLING CATHETER— 510(k) K895772

Substantially Equivalent

Exel Intl.

FDA 510(k) clearance K895772 for EXEL INDWELLING CATHETER, Substantially Equivalent on 1990-02-16. Applicant: Exel Intl.. Device class: 1.

Clearance details

Applicant: Exel Intl.
Product code: Code FDZ
Device class: Class 1
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1989-09-26
Decision date: 1990-02-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Culver City, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FDZ

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K963659 — EXEL I.V. ADMINISTRATION SET1997-12-16
K926119 — EXEL HUBER INFUSION SET ROTATING WING1993-08-11
K904685 — EXEL HUBER INFUSION SET WITHOUT INJECTION SITE (Y)1990-11-21

Data sourced from openFDA. This site is unofficial and independent of the FDA.