FDA 510(k)

HYCOR SENTRY DRUGS OF ABUSE URINE CONTROL:

K-Number: K890957 · 1989-03-09

Decision Date1989-03-09

Product CodeDIF

Advisory CommitteeTX

DecisionSubstantially Equivalent

Device Summary

HYCOR SENTRY DRUGS OF ABUSE URINE CONTROL: 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 1989-03-09 under 510(k) number K890957. The device is classified under product code DIF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYCOR SENTRY DRUGS OF ABUSE URINE CONTROL:?

HYCOR SENTRY DRUGS OF ABUSE URINE CONTROL: is a medical device that received FDA 510(k) clearance on 1989-03-09. The listed applicant is Hycor Biomedical, Inc.. The 510(k) number is K890957.

When did HYCOR SENTRY DRUGS OF ABUSE URINE CONTROL: receive FDA 510(k) clearance?

HYCOR SENTRY DRUGS OF ABUSE URINE CONTROL: received FDA 510(k) clearance on 1989-03-09, under 510(k) number K890957.

Who is the listed applicant for HYCOR SENTRY DRUGS OF ABUSE URINE CONTROL:?

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 SENTRY DRUGS OF ABUSE URINE CONTROL:?

The FDA product code for HYCOR SENTRY DRUGS OF ABUSE URINE CONTROL: is DIF.

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Other records listing Hycor Biomedical, Inc. as applicant

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Related Devices (Code: DIF)

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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.