ADRENOCORTICOTROPIC/ACTH ANALYSIS PRODUCT— 510(k) K926396

Name: FDA 510(k) clearance K926396
Creator: U.S. Food and Drug Administration
Published: 1993-07-27

Substantially Equivalent

Nichols Institute

FDA 510(k) clearance K926396 for ADRENOCORTICOTROPIC/ACTH ANALYSIS PRODUCT, Substantially Equivalent on 1993-07-27. Applicant: Nichols Institute. Device class: 2.

Clearance details

Applicant: Nichols Institute
Product code: Code CKG
Device class: Class 2
Regulation: 21 CFR 862.1025
Advisory panel: Clinical Chemistry
Date received: 1992-12-21
Decision date: 1993-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Juan Capistrano, CA, US

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