INTERFACE PRE BYPASS PRIME FILTER— 510(k) K812240

Name: FDA 510(k) clearance K812240
Creator: U.S. Food and Drug Administration
Published: 1981-08-25

Substantially Equivalent

Medical, Inc.

FDA 510(k) clearance K812240 for INTERFACE PRE BYPASS PRIME FILTER, Substantially Equivalent on 1981-08-25. Applicant: Medical, Inc.. Device class: 2.

Clearance details

Applicant: Medical, Inc.
Product code: Code KRJ
Device class: Class 2
Regulation: 21 CFR 870.4280
Advisory panel: Cardiovascular
Date received: 1981-08-11
Decision date: 1981-08-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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