INTERSEPT* BLOOD FILTER W/ TUBING BYPASS— 510(k) K790435

Substantially Equivalent

Surgikos, Inc.

FDA 510(k) clearance K790435 for INTERSEPT* BLOOD FILTER W/ TUBING BYPASS, Substantially Equivalent on 1979-03-27. Applicant: Surgikos, Inc..

Clearance details

Applicant: Surgikos, Inc.
Product code: Code DTM
Advisory panel: Cardiovascular
Date received: 1979-02-13
Decision date: 1979-03-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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