ANTI-TOXOPLASMA GONDII KIT
K-Number: K842664 · 1984-08-28
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Device Summary
Frequently Asked Questions
What is the ANTI-TOXOPLASMA GONDII KIT?
ANTI-TOXOPLASMA GONDII KIT is a medical device that received FDA 510(k) clearance on 1984-08-28. The listed applicant is Amico Lab, Inc.. The 510(k) number is K842664.
When did ANTI-TOXOPLASMA GONDII KIT receive FDA 510(k) clearance?
ANTI-TOXOPLASMA GONDII KIT received FDA 510(k) clearance on 1984-08-28, under 510(k) number K842664.
Who is the listed applicant for ANTI-TOXOPLASMA GONDII KIT?
The FDA 510(k) record lists Amico Lab, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANTI-TOXOPLASMA GONDII KIT?
The FDA product code for ANTI-TOXOPLASMA GONDII KIT is GLZ.
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 Amico Lab, 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: GLZ)
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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