ALLEGRO ACTH IMMUNOASSAY KIT 65 AND 130 TUBES— 510(k) K882741

Name: FDA 510(k) clearance K882741
Creator: U.S. Food and Drug Administration
Published: 1988-08-30

Substantially Equivalent

Nichols Institute Diagnostics

FDA 510(k) clearance K882741 for ALLEGRO ACTH IMMUNOASSAY KIT 65 AND 130 TUBES, Substantially Equivalent on 1988-08-30. Applicant: Nichols Institute Diagnostics. Device class: 2.

Clearance details

Applicant: Nichols Institute Diagnostics
Product code: Code CKG
Device class: Class 2
Regulation: 21 CFR 862.1025
Advisory panel: Clinical Chemistry
Date received: 1988-07-01
Decision date: 1988-08-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, US

Download summary PDF View on FDA.gov ↗

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