QTEST(TM) PREGNANCY
K-Number: K882086 · 1988-07-28
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Device Summary
Frequently Asked Questions
What is the QTEST(TM) PREGNANCY?
QTEST(TM) PREGNANCY is a medical device that received FDA 510(k) clearance on 1988-07-28. The listed applicant is Quidel Corp.. The 510(k) number is K882086.
When did QTEST(TM) PREGNANCY receive FDA 510(k) clearance?
QTEST(TM) PREGNANCY received FDA 510(k) clearance on 1988-07-28, under 510(k) number K882086.
Who is the listed applicant for QTEST(TM) PREGNANCY?
The FDA 510(k) record lists Quidel Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QTEST(TM) PREGNANCY?
The FDA product code for QTEST(TM) PREGNANCY is JHI.
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 Quidel Corp. 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: JHI)
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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