NEO-PREGNOSTICON DUOCLON TUBE TEST— 510(k) K831339

Substantially Equivalent

Organon, Inc.

FDA 510(k) clearance K831339 for NEO-PREGNOSTICON DUOCLON TUBE TEST, Substantially Equivalent on 1983-06-08. Applicant: Organon, Inc..

Clearance details

Applicant: Organon, Inc.
Product code: Code JHJ
Advisory panel: Clinical Chemistry
Date received: 1983-04-25
Decision date: 1983-06-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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