CAPIOX ARTERIAL FILTER— 510(k) K002026

Substantially Equivalent

Terumo Medical Corp.

FDA 510(k) clearance K002026 for CAPIOX ARTERIAL FILTER, Substantially Equivalent on 2000-09-06. Applicant: Terumo Medical Corp.. Device class: 2.

Clearance details

Applicant: Terumo Medical Corp.
Product code: Code DTM
Device class: Class 2
Regulation: 21 CFR 870.4260
Advisory panel: Cardiovascular
Date received: 2000-07-03
Decision date: 2000-09-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Elkton, MD, US

Download summary PDF View on FDA.gov ↗

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More clearances from Terumo Medical Corp.

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K091329 — PINNACLE DESTINATION PERIPHERAL GUIDING SHEATH2009-05-29

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