AMBERLITE CG50 RESIN, 100-200 MESH— 510(k) K833320

Substantially Equivalent

Biosan Laboratories, Inc.

FDA 510(k) clearance K833320 for AMBERLITE CG50 RESIN, 100-200 MESH, Substantially Equivalent on 1983-12-08. Applicant: Biosan Laboratories, Inc..

Clearance details

Applicant: Biosan Laboratories, Inc.
Product code: Code KEA
Advisory panel: Clinical Chemistry
Date received: 1983-09-26
Decision date: 1983-12-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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