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FDA 510(k)

PF4 IGG

K-Number: K071781 · 2007-12-19

Decision Date2007-12-19
Product CodeLCO
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

PF4 IGG is the device name listed in this FDA 510(k) record. The listed applicant is Genetic Testing Institute. It received FDA 510(k) clearance on 2007-12-19 under 510(k) number K071781. The device is classified under product code LCO. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

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

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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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