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FDA 510(k)

HYCOR ACCUPINCH METHAMPHETAMINE TEST

K-Number: K904115 · 1990-11-28

ApplicantHycor Biomedical, Inc.
Decision Date1990-11-28
Product CodeDKZ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

HYCOR ACCUPINCH METHAMPHETAMINE TEST is the device name listed in this FDA 510(k) record. The listed applicant is Hycor Biomedical, Inc.. It received FDA 510(k) clearance on 1990-11-28 under 510(k) number K904115. The device is classified under product code DKZ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYCOR ACCUPINCH METHAMPHETAMINE TEST?

HYCOR ACCUPINCH METHAMPHETAMINE TEST is a medical device that received FDA 510(k) clearance on 1990-11-28. The listed applicant is Hycor Biomedical, Inc.. The 510(k) number is K904115.

When did HYCOR ACCUPINCH METHAMPHETAMINE TEST receive FDA 510(k) clearance?

HYCOR ACCUPINCH METHAMPHETAMINE TEST received FDA 510(k) clearance on 1990-11-28, under 510(k) number K904115.

Who is the listed applicant for HYCOR ACCUPINCH METHAMPHETAMINE TEST?

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

What is the FDA product code for HYCOR ACCUPINCH METHAMPHETAMINE TEST?

The FDA product code for HYCOR ACCUPINCH METHAMPHETAMINE TEST is DKZ.

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Other records listing Hycor Biomedical, Inc. as applicant

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Related Devices (Code: DKZ)

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.

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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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