ACTH IRMA KIT MITSUBISHI YUKA— 510(k) K910178

Name: FDA 510(k) clearance K910178
Creator: U.S. Food and Drug Administration
Published: 1991-05-22

Substantially Equivalent

Science Regulatory Services Intl.

FDA 510(k) clearance K910178 for ACTH IRMA KIT MITSUBISHI YUKA, Substantially Equivalent on 1991-05-22. Applicant: Science Regulatory Services Intl.. Device class: 2.

Clearance details

Applicant: Science Regulatory Services Intl.
Product code: Code CKG
Device class: Class 2
Regulation: 21 CFR 862.1025
Advisory panel: Clinical Chemistry
Date received: 1991-01-15
Decision date: 1991-05-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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