QAB2A IGG ELISA KIT
K-Number: K020695 · 2002-04-19
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Device Summary
Frequently Asked Questions
What is the QAB2A IGG ELISA KIT?
QAB2A IGG ELISA KIT is a medical device that received FDA 510(k) clearance on 2002-04-19. The listed applicant is Cheshire Diagnostics , Ltd.. The 510(k) number is K020695.
When did QAB2A IGG ELISA KIT receive FDA 510(k) clearance?
QAB2A IGG ELISA KIT received FDA 510(k) clearance on 2002-04-19, under 510(k) number K020695.
Who is the listed applicant for QAB2A IGG ELISA KIT?
The FDA 510(k) record lists Cheshire Diagnostics , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QAB2A IGG ELISA KIT?
The FDA product code for QAB2A IGG ELISA KIT is MSV.
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 Cheshire Diagnostics , Ltd. 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: MSV)
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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