MODIFIED INTERSEPT PEDIATRIC BLOOD FILTER— 510(k) K880671

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..

Clearance details

Applicant: Medtronic Blood Systems, Inc.
Product code: Code DTM
Advisory panel: Cardiovascular
Date received: 1988-02-18
Decision date: 1988-05-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Anaheim, CA, US

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