PF4 IGG
K-Number: K071781 · 2007-12-19
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Device Summary
Frequently Asked Questions
What is the PF4 IGG?
PF4 IGG is a medical device that received FDA 510(k) clearance on 2007-12-19. The listed applicant is Genetic Testing Institute. The 510(k) number is K071781.
When did PF4 IGG receive FDA 510(k) clearance?
PF4 IGG received FDA 510(k) clearance on 2007-12-19, under 510(k) number K071781.
Who is the listed applicant for PF4 IGG?
The FDA 510(k) record lists Genetic Testing Institute as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PF4 IGG?
The FDA product code for PF4 IGG is LCO.
Other records listing Genetic Testing Institute 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: LCO)
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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