PCTE MICROPOROUS MEMBRANE FILTER— 510(k) K870196

Name: FDA 510(k) clearance K870196
Creator: U.S. Food and Drug Administration
Published: 1987-05-12

Substantially Equivalent

Poretics Corp.

FDA 510(k) clearance K870196 for PCTE MICROPOROUS MEMBRANE FILTER, Substantially Equivalent on 1987-05-12. Applicant: Poretics Corp.. Device class: 1.

Clearance details

Applicant: Poretics Corp.
Product code: Code KET
Device class: Class 1
Regulation: 21 CFR 864.3010
Advisory panel: Pathology
Date received: 1987-01-20
Decision date: 1987-05-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Livermore, CA, US

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