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FDA 510(k)

ANTI-CYTOMEGALOVIRUS KIT

K-Number: K842661 · 1985-12-06

Decision Date1985-12-06
Product CodeGQI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANTI-CYTOMEGALOVIRUS KIT is the device name listed in this FDA 510(k) record. The listed applicant is Amico Lab, Inc.. It received FDA 510(k) clearance on 1985-12-06 under 510(k) number K842661. The device is classified under product code GQI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 32 devices →

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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