ABBOTT OVULATION PREDICTOR TEST— 510(k) K890510

Name: FDA 510(k) clearance K890510
Creator: U.S. Food and Drug Administration
Published: 1989-03-24

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K890510 for ABBOTT OVULATION PREDICTOR TEST, Substantially Equivalent on 1989-03-24. Applicant: Abbott Laboratories. Device class: 1.

Clearance details

Applicant: Abbott Laboratories
Product code: Code CEP
Device class: Class 1
Regulation: 21 CFR 862.1485
Advisory panel: Clinical Chemistry
Date received: 1989-02-01
Decision date: 1989-03-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Abbott Park, IL, US

Download summary PDF View on FDA.gov ↗

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