Scimed(R) Dispatch(Tm) Coronary Infusion Catheter

FDA 510(k) K932616 · Scimed Life Systems, Inc.

Substantially Equivalent

510(k) numberK932616

Submission

Device name
Scimed(R) Dispatch(Tm) Coronary Infusion Catheter
Applicant
Scimed Life Systems, Inc.
Maple Grove, MN, US
Received
June 1, 1993
Decision date
December 15, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KRA – Catheter, Continuous Flush
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1210
Specialty
Cardiovascular

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K231279Peregrine System Infusion Catheter 4-7 mm, Peregrine System Infusion Catheter 3-4 mmKRA · Traditional Ablative Solutions, Inc.07/05/2023SE
K231148ScleroSafe™ 150 mm, ScleroSafe™ 350 mmKRA · Traditional Vvt Medical , Ltd.06/20/2023SE
K230957TriSalus TriNav® LV Infusion SystemKRA · Traditional Trisalus Life Sciences05/02/2023SE
K223139Wallaby 017 Micro CatheterKRA · Traditional Wallaby Medical04/25/2023SE

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Questions and answers

When was Scimed(R) Dispatch(Tm) Coronary Infusion Catheter cleared by the FDA?

Scimed(R) Dispatch(Tm) Coronary Infusion Catheter (K932616) received a 510(k) decision of Substantially Equivalent on December 15, 1993, 197 days after the submission was received.

What is the product code of K932616?

The FDA product code is KRA – Catheter, Continuous Flush, a Class II (moderate risk) device regulated under 21 CFR 870.1210.