HYCOR SENTRY(TM) DRUGS OF ABUSE URINE CALIBRATORS
K-Number: K893815 · 1989-07-25
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Device Summary
Frequently Asked Questions
What is the HYCOR SENTRY(TM) DRUGS OF ABUSE URINE CALIBRATORS?
HYCOR SENTRY(TM) DRUGS OF ABUSE URINE CALIBRATORS is a medical device that received FDA 510(k) clearance on 1989-07-25. The listed applicant is Hycor Biomedical, Inc.. The 510(k) number is K893815.
When did HYCOR SENTRY(TM) DRUGS OF ABUSE URINE CALIBRATORS receive FDA 510(k) clearance?
HYCOR SENTRY(TM) DRUGS OF ABUSE URINE CALIBRATORS received FDA 510(k) clearance on 1989-07-25, under 510(k) number K893815.
Who is the listed applicant for HYCOR SENTRY(TM) DRUGS OF ABUSE URINE CALIBRATORS?
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(TM) DRUGS OF ABUSE URINE CALIBRATORS?
The FDA product code for HYCOR SENTRY(TM) DRUGS OF ABUSE URINE CALIBRATORS is DKB.
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 Hycor Biomedical, 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.
Related Devices (Code: DKB)
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
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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