LOGIQ 1000 DIAGNOSTIC ULTRSOUND SYSTEM
K-Number: K960527 · 1997-09-08
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Device Summary
Frequently Asked Questions
What is the LOGIQ 1000 DIAGNOSTIC ULTRSOUND SYSTEM?
LOGIQ 1000 DIAGNOSTIC ULTRSOUND SYSTEM is a medical device that received FDA 510(k) clearance on 1997-09-08. The listed applicant is GE Medical Systems. The 510(k) number is K960527.
When did LOGIQ 1000 DIAGNOSTIC ULTRSOUND SYSTEM receive FDA 510(k) clearance?
LOGIQ 1000 DIAGNOSTIC ULTRSOUND SYSTEM received FDA 510(k) clearance on 1997-09-08, under 510(k) number K960527.
Who is the listed applicant for LOGIQ 1000 DIAGNOSTIC ULTRSOUND SYSTEM?
The FDA 510(k) record lists GE Medical Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LOGIQ 1000 DIAGNOSTIC ULTRSOUND SYSTEM?
The FDA product code for LOGIQ 1000 DIAGNOSTIC ULTRSOUND SYSTEM 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 Medical Systems 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.
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