FDA 510(k)

WH ACCU TEST PREGNANCY TEST

K-Number: K012284 · 2001-08-28

Decision Date2001-08-28

Product CodeJHI

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

WH ACCU TEST PREGNANCY TEST is the device name listed in this FDA 510(k) record. The listed applicant is W.H.P.M., Inc.. It received FDA 510(k) clearance on 2001-08-28 under 510(k) number K012284. 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 WH ACCU TEST PREGNANCY TEST?

WH ACCU TEST PREGNANCY TEST is a medical device that received FDA 510(k) clearance on 2001-08-28. The listed applicant is W.H.P.M., Inc.. The 510(k) number is K012284.

When did WH ACCU TEST PREGNANCY TEST receive FDA 510(k) clearance?

WH ACCU TEST PREGNANCY TEST received FDA 510(k) clearance on 2001-08-28, under 510(k) number K012284.

Who is the listed applicant for WH ACCU TEST PREGNANCY TEST?

The FDA 510(k) record lists W.H.P.M., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WH ACCU TEST PREGNANCY TEST?

The FDA product code for WH ACCU TEST PREGNANCY TEST is JHI.

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Related Devices (Code: JHI)

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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.