NIKKISO PARALLEL FLOW DIALYZERS— 510(k) K801065

Name: FDA 510(k) clearance K801065
Creator: U.S. Food and Drug Administration
Published: 1980-08-07

Substantially Equivalent

Int'L Marketing & Sales Corp.

FDA 510(k) clearance K801065 for NIKKISO PARALLEL FLOW DIALYZERS, Substantially Equivalent on 1980-08-07. Applicant: Int'L Marketing & Sales Corp.. Device class: 2.

Clearance details

Applicant: Int'L Marketing & Sales Corp.
Product code: Code FTG
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 1980-05-06
Decision date: 1980-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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