Speedlyser Infusion Catheter Kit

FDA 510(k) K033443 · AngioDynamics, Inc.

Unknown

510(k) numberK033443

Submission

Device name
Speedlyser Infusion Catheter Kit
Applicant
AngioDynamics, Inc.
Queensburgy, NY, US
Received
October 29, 2003
Decision date
November 19, 2003
Decision
Unknown (SEKD)
Type
Special 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
QEY – Mechanical Thrombolysis Catheter
Device class
Class II (moderate risk)
Regulation
21 CFR 870.5150
Specialty
Cardiovascular

To mechanically disrupt thrombus and/or debris in the peripheral vasculature.

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Questions and answers

When was Speedlyser Infusion Catheter Kit cleared by the FDA?

Speedlyser Infusion Catheter Kit (K033443) received a 510(k) decision of Unknown on November 19, 2003, 21 days after the submission was received.

What is the product code of K033443?

The FDA product code is QEY – Mechanical Thrombolysis Catheter, a Class II (moderate risk) device regulated under 21 CFR 870.5150.