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FDA 510(k)

CLEARVIEW CHLAMYDIA

K-Number: K895280 · 1990-01-29

ApplicantUnipath , Ltd.
Decision Date1990-01-29
Product CodeLJC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CLEARVIEW CHLAMYDIA is the device name listed in this FDA 510(k) record. The listed applicant is Unipath , Ltd.. It received FDA 510(k) clearance on 1990-01-29 under 510(k) number K895280. The device is classified under product code LJC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEARVIEW CHLAMYDIA?

CLEARVIEW CHLAMYDIA is a medical device that received FDA 510(k) clearance on 1990-01-29. The listed applicant is Unipath , Ltd.. The 510(k) number is K895280.

When did CLEARVIEW CHLAMYDIA receive FDA 510(k) clearance?

CLEARVIEW CHLAMYDIA received FDA 510(k) clearance on 1990-01-29, under 510(k) number K895280.

Who is the listed applicant for CLEARVIEW CHLAMYDIA?

The FDA 510(k) record lists Unipath , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLEARVIEW CHLAMYDIA?

The FDA product code for CLEARVIEW CHLAMYDIA is LJC.

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Other records listing Unipath , Ltd. as applicant

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Related Devices (Code: LJC)

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.

K032330CT OIAThermo Biostar, Inc.K033865IDEIA PCE CHLAMYDIADakocytomation, Ltd.K033079CHLAMYDIA IGG ELISA TEST SYSTEMTrinity Biotech USAK982210MODIFICATION OF SYVA MICROTRAK II CHLAMYDIA EIADade Behring, Inc.K962558CHLAMYDIA IGG ELISA TEST SYSTEMArmkel, LLCK960850ACCESS CHLAMYDIA ASSAYBio-Rad Laboratories, Inc.

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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