MODIFIED BIO. HEMODIALYSIS & HD-1000 DISP. CART.— 510(k) K870270

Name: FDA 510(k) clearance K870270
Creator: U.S. Food and Drug Administration
Published: 1987-02-25

Substantially Equivalent

Ash Medical Systems, Inc.

FDA 510(k) clearance K870270 for MODIFIED BIO. HEMODIALYSIS & HD-1000 DISP. CART., Substantially Equivalent on 1987-02-25. Applicant: Ash Medical Systems, Inc.. Device class: 2.

Clearance details

Applicant: Ash Medical Systems, Inc.
Product code: Code FKT
Device class: Class 2
Regulation: 21 CFR 876.5600
Advisory panel: Gastroenterology, Urology
Date received: 1987-01-27
Decision date: 1987-02-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Lafayette, IN, US

Download summary PDF View on FDA.gov ↗

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