ANTI-CYTOMEGALOVIRUS KIT
K-Number: K842661 · 1985-12-06
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Device Summary
Frequently Asked Questions
What is the ANTI-CYTOMEGALOVIRUS KIT?
ANTI-CYTOMEGALOVIRUS KIT is a medical device that received FDA 510(k) clearance on 1985-12-06. The listed applicant is Amico Lab, Inc.. The 510(k) number is K842661.
When did ANTI-CYTOMEGALOVIRUS KIT receive FDA 510(k) clearance?
ANTI-CYTOMEGALOVIRUS KIT received FDA 510(k) clearance on 1985-12-06, under 510(k) number K842661.
Who is the listed applicant for ANTI-CYTOMEGALOVIRUS 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-CYTOMEGALOVIRUS KIT?
The FDA product code for ANTI-CYTOMEGALOVIRUS KIT is GQI.
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: GQI)
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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