EBV-VCA IGG ELISA TEST, MODEL EBG-100
K-Number: K020706 · 2002-06-13
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Device Summary
Frequently Asked Questions
What is the EBV-VCA IGG ELISA TEST, MODEL EBG-100?
EBV-VCA IGG ELISA TEST, MODEL EBG-100 is a medical device that received FDA 510(k) clearance on 2002-06-13. The listed applicant is Pan Bio Pty. , Ltd.. The 510(k) number is K020706.
When did EBV-VCA IGG ELISA TEST, MODEL EBG-100 receive FDA 510(k) clearance?
EBV-VCA IGG ELISA TEST, MODEL EBG-100 received FDA 510(k) clearance on 2002-06-13, under 510(k) number K020706.
Who is the listed applicant for EBV-VCA IGG ELISA TEST, MODEL EBG-100?
The FDA 510(k) record lists Pan Bio Pty. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EBV-VCA IGG ELISA TEST, MODEL EBG-100?
The FDA product code for EBV-VCA IGG ELISA TEST, MODEL EBG-100 is GNP.
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 Pan Bio Pty. , 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: GNP)
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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