MODIFIED INTERSEPT PEDIATRIC BLOOD FILTER— 510(k) K880671

Name: FDA 510(k) clearance K880671
Creator: U.S. Food and Drug Administration
Published: 1988-05-06

Substantially Equivalent

Medtronic Blood Systems, Inc.

FDA 510(k) clearance K880671 for MODIFIED INTERSEPT PEDIATRIC BLOOD FILTER, Substantially Equivalent on 1988-05-06. Applicant: Medtronic Blood Systems, Inc.. Device class: 2.

Clearance details

Applicant: Medtronic Blood Systems, Inc.
Product code: Code DTM
Device class: Class 2
Regulation: 21 CFR 870.4260
Advisory panel: Cardiovascular
Date received: 1988-02-18
Decision date: 1988-05-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Anaheim, CA, 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.