ARTERIAL BUBBLE TRAP K-20— 510(k) K803102

Name: FDA 510(k) clearance K803102
Creator: U.S. Food and Drug Administration
Published: 1980-12-22

Substantially Equivalent

Delta Medical Industries

FDA 510(k) clearance K803102 for ARTERIAL BUBBLE TRAP K-20, Substantially Equivalent on 1980-12-22. Applicant: Delta Medical Industries. Device class: 2.

Clearance details

Applicant: Delta Medical Industries
Product code: Code KRL
Device class: Class 2
Regulation: 21 CFR 870.4205
Advisory panel: Cardiovascular
Date received: 1980-12-09
Decision date: 1980-12-22
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.