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FDA 510(k)

Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate Tubing

K-Number: K243418 · 2024-12-02

ApplicantMicro Therapeutics, Inc. d/b/a ev3 Neurovascular
Decision Date2024-12-02
Product CodeJCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate Tubing is a medical device manufactured by Micro Therapeutics, Inc. d/b/a ev3 Neurovascular. It received FDA 510(k) clearance on 2024-12-02 under approval number K243418. The device is classified under product code JCX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate Tubing?

Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate Tubing is a medical device that received FDA 510(k) clearance on 2024-12-02. It is manufactured by Micro Therapeutics, Inc. d/b/a ev3 Neurovascular. The 510(k) number is K243418.

When was Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate Tubing approved by the FDA?

Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate Tubing received FDA 510(k) clearance on 2024-12-02, under approval number K243418.

What company makes Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate Tubing?

Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate Tubing is manufactured by Micro Therapeutics, Inc. d/b/a ev3 Neurovascular.

What is the FDA product code for Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate Tubing?

The FDA product code for Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate Tubing is JCX.

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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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