PENTOBARBITAL TOXICOLOGY CONTROL
K-Number: K831739 · 1983-07-06
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Device Summary
Frequently Asked Questions
What is the PENTOBARBITAL TOXICOLOGY CONTROL?
PENTOBARBITAL TOXICOLOGY CONTROL is a medical device that received FDA 510(k) clearance on 1983-07-06. The listed applicant is Utak Laboratories, Inc.. The 510(k) number is K831739.
When did PENTOBARBITAL TOXICOLOGY CONTROL receive FDA 510(k) clearance?
PENTOBARBITAL TOXICOLOGY CONTROL received FDA 510(k) clearance on 1983-07-06, under 510(k) number K831739.
Who is the listed applicant for PENTOBARBITAL 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 PENTOBARBITAL TOXICOLOGY CONTROL?
The FDA product code for PENTOBARBITAL 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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