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FDA 510(k)

Penumbra System (Reperfusion Catheter RED 72)

K-Number: K242104 · 2025-02-13

ApplicantPenumbra, Inc.
Decision Date2025-02-13
Product CodeNRY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Penumbra System (Reperfusion Catheter RED 72) is a medical device manufactured by Penumbra, Inc.. It received FDA 510(k) clearance on 2025-02-13 under approval number K242104. The device is classified under product code NRY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Penumbra System (Reperfusion Catheter RED 72)?

Penumbra System (Reperfusion Catheter RED 72) is a medical device that received FDA 510(k) clearance on 2025-02-13. It is manufactured by Penumbra, Inc.. The 510(k) number is K242104.

When was Penumbra System (Reperfusion Catheter RED 72) approved by the FDA?

Penumbra System (Reperfusion Catheter RED 72) received FDA 510(k) clearance on 2025-02-13, under approval number K242104.

What company makes Penumbra System (Reperfusion Catheter RED 72)?

Penumbra System (Reperfusion Catheter RED 72) is manufactured by Penumbra, Inc..

What is the FDA product code for Penumbra System (Reperfusion Catheter RED 72)?

The FDA product code for Penumbra System (Reperfusion Catheter RED 72) is NRY.

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Other Devices by Penumbra, Inc.

K161506Penumbra Aspiration System K161640Penumbra System ACE 68 Reperfusion Catheter K161523INDIGO Aspiration System K161064Penumbra System ACE 68 Reperfusion Catheter K160449Penumbra System, Penumbra Pump MAX K160533Penumbra Embolectomy Aspiration System (INDIGOTM Aspiration System)

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Related Devices (Code: NRY)

K161879Solitaire Platinum Revascularization DeviceMicro Therapeutics, Inc. d/b/a ev3 Neurovascular K161640Penumbra System ACE 68 Reperfusion CatheterPenumbra, Inc. K161064Penumbra System ACE 68 Reperfusion CatheterPenumbra, Inc. K160449Penumbra System, Penumbra Pump MAXPenumbra, Inc. K152541Penumbra System ACE 64 and ACE 68 Reperfusion CathetersPenumbra, Inc. K172448Riptide Aspiration SystemMicro Therapeutics, Inc. d/b/a ev3 Neurovascular

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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