MODIF. OF EMIT URINE BENZODIAZEPINE
K-Number: K833578 · 1984-01-26
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Device Summary
Frequently Asked Questions
What is the MODIF. OF EMIT URINE BENZODIAZEPINE?
MODIF. OF EMIT URINE BENZODIAZEPINE is a medical device that received FDA 510(k) clearance on 1984-01-26. The listed applicant is Syva Co.. The 510(k) number is K833578.
When did MODIF. OF EMIT URINE BENZODIAZEPINE receive FDA 510(k) clearance?
MODIF. OF EMIT URINE BENZODIAZEPINE received FDA 510(k) clearance on 1984-01-26, under 510(k) number K833578.
Who is the listed applicant for MODIF. OF EMIT URINE BENZODIAZEPINE?
The FDA 510(k) record lists Syva Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIF. OF EMIT URINE BENZODIAZEPINE?
The FDA product code for MODIF. OF EMIT URINE BENZODIAZEPINE is JXM.
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 Syva Co. 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: JXM)
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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