SERUM CLONAZEPAM TOXICOLOGY CONTROL
K-Number: K862421 · 1986-11-05
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Device Summary
Frequently Asked Questions
What is the SERUM CLONAZEPAM TOXICOLOGY CONTROL?
SERUM CLONAZEPAM TOXICOLOGY CONTROL is a medical device that received FDA 510(k) clearance on 1986-11-05. The listed applicant is Utak Laboratories, Inc.. The 510(k) number is K862421.
When did SERUM CLONAZEPAM TOXICOLOGY CONTROL receive FDA 510(k) clearance?
SERUM CLONAZEPAM TOXICOLOGY CONTROL received FDA 510(k) clearance on 1986-11-05, under 510(k) number K862421.
Who is the listed applicant for SERUM CLONAZEPAM TOXICOLOGY CONTROL?
The FDA 510(k) record lists Utak Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SERUM CLONAZEPAM TOXICOLOGY CONTROL?
The FDA product code for SERUM CLONAZEPAM TOXICOLOGY CONTROL is LAS.
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 Utak Laboratories, 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: LAS)
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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