PEDIATRIC ARTERIAL BLOOD FILTER— 510(k) K810068

Name: FDA 510(k) clearance K810068
Creator: U.S. Food and Drug Administration
Published: 1981-01-22

Substantially Equivalent

Delta Medical Industries

FDA 510(k) clearance K810068 for PEDIATRIC ARTERIAL BLOOD FILTER, Substantially Equivalent on 1981-01-22. Applicant: Delta Medical Industries. Device class: 2.

Clearance details

Applicant: Delta Medical Industries
Product code: Code DTM
Device class: Class 2
Regulation: 21 CFR 870.4260
Advisory panel: Cardiovascular
Date received: 1981-01-13
Decision date: 1981-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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