KIDNEY, ARTIFICIAL, C-DAK 1.5— 510(k) K781238

Substantially Equivalent

Cordis Corp.

FDA 510(k) clearance K781238 for KIDNEY, ARTIFICIAL, C-DAK 1.5, Substantially Equivalent on 1978-08-31. Applicant: Cordis Corp..

Clearance details

Applicant: Cordis Corp.
Product code: Code DJC
Advisory panel: Clinical Toxicology
Date received: 1978-07-20
Decision date: 1978-08-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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