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# Penumbra Expanded Indication for Aspiration Device
- URL: https://www.fdaweb.com/penumbra-expanded-indication-for-aspiration-device/
- Published: 2020-01-09T12:00:00.000Z
- Updated: 2026-09-14T15:58:00.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5145813

FDA has cleared a Penumbra 510(k) for an expanded indication for its Indigo Aspiration System — treating pulmonary embolisms. Previously, the device was cleared for removing fresh, soft emboli and thrombi from vessels of the peripheral arterial and venous systems. The company says it uses its proprietary Penumbra Engine aspiration source to deliver continuous vacuum suction to the Indigo System Aspiration Catheters to address emboli and thrombus in vessels of various sizes.