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FDA 510(k)

ANTI-CHLAMYDIA TRACHOMATIS KIT

K-Number: K842658 · 1984-10-01

Decision Date1984-10-01
Product CodeLJP
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANTI-CHLAMYDIA TRACHOMATIS 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 1984-10-01 under 510(k) number K842658. The device is classified under product code LJP. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTI-CHLAMYDIA TRACHOMATIS KIT?

ANTI-CHLAMYDIA TRACHOMATIS KIT is a medical device that received FDA 510(k) clearance on 1984-10-01. The listed applicant is Amico Lab, Inc.. The 510(k) number is K842658.

When did ANTI-CHLAMYDIA TRACHOMATIS KIT receive FDA 510(k) clearance?

ANTI-CHLAMYDIA TRACHOMATIS KIT received FDA 510(k) clearance on 1984-10-01, under 510(k) number K842658.

Who is the listed applicant for ANTI-CHLAMYDIA TRACHOMATIS 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-CHLAMYDIA TRACHOMATIS KIT?

The FDA product code for ANTI-CHLAMYDIA TRACHOMATIS KIT is LJP.

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.

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Related Devices (Code: LJP)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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