ARANTROL— 510(k) K780835

Substantially Equivalent

Aranco Diagnostic Laboratories, Inc.

FDA 510(k) clearance K780835 for ARANTROL, Substantially Equivalent on 1978-06-22. Applicant: Aranco Diagnostic Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Aranco Diagnostic Laboratories, Inc.
Product code: Code JPK
Device class: Class 2
Regulation: 21 CFR 864.8625
Advisory panel: Hematology
Date received: 1978-05-23
Decision date: 1978-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.