FORETEL, COLOR OVULATION TEST
K-Number: K860828 · 1986-08-04
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Device Summary
Frequently Asked Questions
What is the FORETEL, COLOR OVULATION TEST?
FORETEL, COLOR OVULATION TEST is a medical device that received FDA 510(k) clearance on 1986-08-04. The listed applicant is Nms Pharmaceuticals, Inc.. The 510(k) number is K860828.
When did FORETEL, COLOR OVULATION TEST receive FDA 510(k) clearance?
FORETEL, COLOR OVULATION TEST received FDA 510(k) clearance on 1986-08-04, under 510(k) number K860828.
Who is the listed applicant for FORETEL, COLOR OVULATION TEST?
The FDA 510(k) record lists Nms Pharmaceuticals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FORETEL, COLOR OVULATION TEST?
The FDA product code for FORETEL, COLOR OVULATION 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 Nms Pharmaceuticals, Inc. 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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