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FDA 510(k)

ONE STEP HCG PREGNANCY TEST

K-Number: K062703 · 2007-07-23

Decision Date2007-07-23
Product CodeLCX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ONE STEP HCG PREGNANCY TEST is the device name listed in this FDA 510(k) record. The listed applicant is Ai DE Diagnostic Co., Ltd.. It received FDA 510(k) clearance on 2007-07-23 under 510(k) number K062703. The device is classified under product code LCX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ONE STEP HCG PREGNANCY TEST?

ONE STEP HCG PREGNANCY TEST is a medical device that received FDA 510(k) clearance on 2007-07-23. The listed applicant is Ai DE Diagnostic Co., Ltd.. The 510(k) number is K062703.

When did ONE STEP HCG PREGNANCY TEST receive FDA 510(k) clearance?

ONE STEP HCG PREGNANCY TEST received FDA 510(k) clearance on 2007-07-23, under 510(k) number K062703.

Who is the listed applicant for ONE STEP HCG PREGNANCY TEST?

The FDA 510(k) record lists Ai DE Diagnostic Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ONE STEP HCG PREGNANCY TEST?

The FDA product code for ONE STEP HCG PREGNANCY TEST 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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