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FDA 510(k)

QTEST PREGNANCY TEST CONTROL

K-Number: K883741 · 1988-10-03

ApplicantQuidel Corp.
Decision Date1988-10-03
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

QTEST PREGNANCY TEST CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Quidel Corp.. It received FDA 510(k) clearance on 1988-10-03 under 510(k) number K883741. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QTEST PREGNANCY TEST CONTROL?

QTEST PREGNANCY TEST CONTROL is a medical device that received FDA 510(k) clearance on 1988-10-03. The listed applicant is Quidel Corp.. The 510(k) number is K883741.

When did QTEST PREGNANCY TEST CONTROL receive FDA 510(k) clearance?

QTEST PREGNANCY TEST CONTROL received FDA 510(k) clearance on 1988-10-03, under 510(k) number K883741.

Who is the listed applicant for QTEST PREGNANCY TEST CONTROL?

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 PREGNANCY TEST CONTROL?

The FDA product code for QTEST PREGNANCY TEST CONTROL is JJX.

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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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