PREGNANCY TEST KIT, ANSWER
K-Number: K772359 · 1978-01-05
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Device Summary
Frequently Asked Questions
What is the PREGNANCY TEST KIT, ANSWER?
PREGNANCY TEST KIT, ANSWER is a medical device that received FDA 510(k) clearance on 1978-01-05. The listed applicant is Diagnostic Testing, Inc.. The 510(k) number is K772359.
When did PREGNANCY TEST KIT, ANSWER receive FDA 510(k) clearance?
PREGNANCY TEST KIT, ANSWER received FDA 510(k) clearance on 1978-01-05, under 510(k) number K772359.
Who is the listed applicant for PREGNANCY TEST KIT, ANSWER?
The FDA 510(k) record lists Diagnostic Testing, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PREGNANCY TEST KIT, ANSWER?
The FDA product code for PREGNANCY TEST KIT, ANSWER 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.
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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