ERYTHROPOIETIN EIA— 510(k) K833957

Substantially Equivalent

Jcl Clinical Research Corp.

FDA 510(k) clearance K833957 for ERYTHROPOIETIN EIA, Substantially Equivalent on 1984-03-23. Applicant: Jcl Clinical Research Corp.. Device class: 2.

Clearance details

Applicant: Jcl Clinical Research Corp.
Product code: Code GGT
Device class: Class 2
Regulation: 21 CFR 864.7250
Advisory panel: Hematology
Date received: 1983-11-16
Decision date: 1984-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.