LOGIQ P9 and LOGIQ P7
K-Number: K163596 · 2017-02-10
Device Summary
Frequently Asked Questions
What is the LOGIQ P9 and LOGIQ P7?
LOGIQ P9 and LOGIQ P7 is a medical device that received FDA 510(k) clearance on 2017-02-10. The listed applicant is GE Healthcare. The 510(k) number is K163596.
When did LOGIQ P9 and LOGIQ P7 receive FDA 510(k) clearance?
LOGIQ P9 and LOGIQ P7 received FDA 510(k) clearance on 2017-02-10, under 510(k) number K163596.
Who is the listed applicant for LOGIQ P9 and LOGIQ P7?
The FDA 510(k) record lists GE Healthcare as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LOGIQ P9 and LOGIQ P7?
The FDA product code for LOGIQ P9 and LOGIQ P7 is IYN.
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 GE Healthcare 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: IYN)
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.