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FDA 510(k)

HYCOR ACCUPINCH COCAINE TEST

K-Number: K896937 · 1990-03-06

ApplicantHycor Biomedical, Inc.
Decision Date1990-03-06
Product CodeDIO
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

HYCOR ACCUPINCH COCAINE 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 1990-03-06 under 510(k) number K896937. The device is classified under product code DIO. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYCOR ACCUPINCH COCAINE TEST?

HYCOR ACCUPINCH COCAINE TEST is a medical device that received FDA 510(k) clearance on 1990-03-06. The listed applicant is Hycor Biomedical, Inc.. The 510(k) number is K896937.

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

HYCOR ACCUPINCH COCAINE TEST received FDA 510(k) clearance on 1990-03-06, under 510(k) number K896937.

Who is the listed applicant for HYCOR ACCUPINCH COCAINE 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 COCAINE TEST?

The FDA product code for HYCOR ACCUPINCH COCAINE TEST is DIO.

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Related Devices (Code: DIO)

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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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