RIGHT-DAY OVULATION HOME TEST— 510(k) K861354

Substantially Equivalent

Leeco Diagnostics, Inc.

FDA 510(k) clearance K861354 for RIGHT-DAY OVULATION HOME TEST, Substantially Equivalent on 1986-09-16. Applicant: Leeco Diagnostics, Inc..

Clearance details

Applicant: Leeco Diagnostics, Inc.
Product code: Code CEP
Advisory panel: Clinical Chemistry
Date received: 1986-04-10
Decision date: 1986-09-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Southfield, MI, US

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