HOME PREGNANCY TEST KIT HPK #1
K-Number: K831051 · 1983-05-18
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Device Summary
Frequently Asked Questions
What is the HOME PREGNANCY TEST KIT HPK #1?
HOME PREGNANCY TEST KIT HPK #1 is a medical device that received FDA 510(k) clearance on 1983-05-18. The listed applicant is Quidel Corp.. The 510(k) number is K831051.
When did HOME PREGNANCY TEST KIT HPK #1 receive FDA 510(k) clearance?
HOME PREGNANCY TEST KIT HPK #1 received FDA 510(k) clearance on 1983-05-18, under 510(k) number K831051.
Who is the listed applicant for HOME PREGNANCY TEST KIT HPK #1?
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 HOME PREGNANCY TEST KIT HPK #1?
The FDA product code for HOME PREGNANCY TEST KIT HPK #1 is LCX.
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: LCX)
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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