IMMUNOCOAT PROGESTERONE RADIOIMMUNOASSAY KIT— 510(k) K894049

Name: FDA 510(k) clearance K894049
Creator: U.S. Food and Drug Administration
Published: 1989-09-08

Substantially Equivalent

Pantex, Div. Bio-Analysis, Inc.

FDA 510(k) clearance K894049 for IMMUNOCOAT PROGESTERONE RADIOIMMUNOASSAY KIT, Substantially Equivalent on 1989-09-08. Applicant: Pantex, Div. Bio-Analysis, Inc.. Device class: 1.

Clearance details

Applicant: Pantex, Div. Bio-Analysis, Inc.
Product code: Code JLS
Device class: Class 1
Regulation: 21 CFR 862.1620
Advisory panel: Clinical Chemistry
Date received: 1989-06-07
Decision date: 1989-09-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Monica, CA, US

Download summary PDF View on FDA.gov ↗

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