ABBOTT OVULATION PREDICTOR TEST
K-Number: K890510 · 1989-03-24
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Device Summary
Frequently Asked Questions
What is the ABBOTT OVULATION PREDICTOR TEST?
ABBOTT OVULATION PREDICTOR TEST is a medical device that received FDA 510(k) clearance on 1989-03-24. The listed applicant is Abbott Laboratories. The 510(k) number is K890510.
When did ABBOTT OVULATION PREDICTOR TEST receive FDA 510(k) clearance?
ABBOTT OVULATION PREDICTOR TEST received FDA 510(k) clearance on 1989-03-24, under 510(k) number K890510.
Who is the listed applicant for ABBOTT OVULATION PREDICTOR TEST?
The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ABBOTT OVULATION PREDICTOR TEST?
The FDA product code for ABBOTT OVULATION PREDICTOR TEST is CEP.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Abbott Laboratories as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: CEP)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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