FERTELL FEMALE FERTILITY TEST— 510(k) K032002

Substantially Equivalent

Genosis, Inc.

FDA 510(k) clearance K032002 for FERTELL FEMALE FERTILITY TEST, Substantially Equivalent on 2003-10-30. Applicant: Genosis, Inc..

Clearance details

Applicant: Genosis, Inc.
Product code: Code NGA
Advisory panel: Clinical Chemistry
Date received: 2003-06-27
Decision date: 2003-10-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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