Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate Tubing
K-Number: K243418 · 2024-12-02
Device Summary
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. The listed applicant is Micro Therapeutics, Inc. d/b/a ev3 Neurovascular. The 510(k) number is K243418.
When did Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate Tubing receive FDA 510(k) clearance?
Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate Tubing received FDA 510(k) clearance on 2024-12-02, under 510(k) number K243418.
Who is the listed applicant for Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate Tubing?
The FDA 510(k) record lists Micro Therapeutics, Inc. d/b/a ev3 Neurovascular as the applicant. This does not by itself establish the device manufacturer.
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.
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 Micro Therapeutics, Inc. d/b/a ev3 Neurovascular 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: JCX)
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.