LOGIQ Totus
K-Number: K232381 · 2023-12-07
Device Summary
Frequently Asked Questions
What is the LOGIQ Totus?
LOGIQ Totus is a medical device that received FDA 510(k) clearance on 2023-12-07. The listed applicant is GE Medical Systems Ultrasound and Primary Care Diagnostics. The 510(k) number is K232381.
When did LOGIQ Totus receive FDA 510(k) clearance?
LOGIQ Totus received FDA 510(k) clearance on 2023-12-07, under 510(k) number K232381.
Who is the listed applicant for LOGIQ Totus?
The FDA 510(k) record lists GE Medical Systems Ultrasound and Primary Care Diagnostics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LOGIQ Totus?
The FDA product code for LOGIQ Totus is IYN.
Other records listing GE Medical Systems Ultrasound and Primary Care Diagnostics 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.