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FDA 510(k)

EXCEL ONE STEP URINE HCG PREGNANCY DIPSTICK TEST

K-Number: K970424 · 1997-03-06

Decision Date1997-03-06
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EXCEL ONE STEP URINE HCG PREGNANCY DIPSTICK TEST is the device name listed in this FDA 510(k) record. The listed applicant is Excel Scientific, Inc.. It received FDA 510(k) clearance on 1997-03-06 under 510(k) number K970424. 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 EXCEL ONE STEP URINE HCG PREGNANCY DIPSTICK TEST?

EXCEL ONE STEP URINE HCG PREGNANCY DIPSTICK TEST is a medical device that received FDA 510(k) clearance on 1997-03-06. The listed applicant is Excel Scientific, Inc.. The 510(k) number is K970424.

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

EXCEL ONE STEP URINE HCG PREGNANCY DIPSTICK TEST received FDA 510(k) clearance on 1997-03-06, under 510(k) number K970424.

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

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

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

The FDA product code for EXCEL ONE STEP URINE HCG PREGNANCY DIPSTICK 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.

Other records listing Excel Scientific, Inc. 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.

View all 8 devices →

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

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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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