MAXXUS
K-Number: K924498 · 1992-12-03
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Device Summary
Frequently Asked Questions
What is the MAXXUS?
MAXXUS is a medical device that received FDA 510(k) clearance on 1992-12-03. The listed applicant is GE Medical Systems. The 510(k) number is K924498.
When did MAXXUS receive FDA 510(k) clearance?
MAXXUS received FDA 510(k) clearance on 1992-12-03, under 510(k) number K924498.
Who is the listed applicant for MAXXUS?
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 MAXXUS?
The FDA product code for MAXXUS is KPS.
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: KPS)
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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