IN-HOME EARLY PREGNANCY TEST KIT— 510(k) K802334

Substantially Equivalent

Health Diagnostics Corp.

FDA 510(k) clearance K802334 for IN-HOME EARLY PREGNANCY TEST KIT, Substantially Equivalent on 1980-10-10. Applicant: Health Diagnostics Corp..

Clearance details

Applicant: Health Diagnostics Corp.
Product code: Code JHJ
Advisory panel: Clinical Chemistry
Date received: 1980-09-23
Decision date: 1980-10-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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