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FDA 510(k)

MAINLINE MAXIE HCG URINE PREGNANCY TEST

K-Number: K031445 · 2003-07-01

Decision Date2003-07-01
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MAINLINE MAXIE HCG URINE PREGNANCY TEST is the device name listed in this FDA 510(k) record. The listed applicant is Mainline Technology, Inc.. It received FDA 510(k) clearance on 2003-07-01 under 510(k) number K031445. The device is classified under product code JHI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAINLINE MAXIE HCG URINE PREGNANCY TEST?

MAINLINE MAXIE HCG URINE PREGNANCY TEST is a medical device that received FDA 510(k) clearance on 2003-07-01. The listed applicant is Mainline Technology, Inc.. The 510(k) number is K031445.

When did MAINLINE MAXIE HCG URINE PREGNANCY TEST receive FDA 510(k) clearance?

MAINLINE MAXIE HCG URINE PREGNANCY TEST received FDA 510(k) clearance on 2003-07-01, under 510(k) number K031445.

Who is the listed applicant for MAINLINE MAXIE HCG URINE PREGNANCY TEST?

The FDA 510(k) record lists Mainline Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAINLINE MAXIE HCG URINE PREGNANCY TEST?

The FDA product code for MAINLINE MAXIE HCG URINE PREGNANCY TEST 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.

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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