Accutome, Inc. Doing Business AS Keeler USA - FDA 510(k) Cleared Devi...
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Cleared
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Denied
Accutome, Inc. Doing Business AS Keeler USA has 1 FDA 510(k) cleared medical devices. Based in Malvern, US.
Latest FDA clearance: Jul 2025. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Accutome, Inc. Doing Business AS Keeler USA Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Keeler, Ltd. as regulatory consultant.
1 devices