Shiley Equipment Support Carts ESC-002 & ESCB-02

FDA 510(k) K892446 · Shiley, Inc.

Substantially Equivalent

510(k) numberK892446

Submission

Device name
Shiley Equipment Support Carts ESC-002 & ESCB-02
Applicant
Shiley, Inc.
Irvine, CA, US
Received
April 10, 1989
Decision date
July 14, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KRD – Device, Vascular, For Promoting Embolization
Device class
Class II (moderate risk)
Regulation
21 CFR 870.3300
Specialty
Cardiovascular
Implant
Yes

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K260508LOBO Vascular Occlusion SystemKRD · Traditional Okami Medical, Inc.04/10/2026SE
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K253677Tembo Embolic SystemKRD · Special Instylla, Inc.12/15/2025SE
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K250209Polyvinyl Alcohol Embolic MicrospheresKRD · Traditional Canyon Medical, Inc.09/23/2025SE
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Questions and answers

When was Shiley Equipment Support Carts ESC-002 & ESCB-02 cleared by the FDA?

Shiley Equipment Support Carts ESC-002 & ESCB-02 (K892446) received a 510(k) decision of Substantially Equivalent on July 14, 1989, 95 days after the submission was received.

What is the product code of K892446?

The FDA product code is KRD – Device, Vascular, For Promoting Embolization, a Class II (moderate risk) device regulated under 21 CFR 870.3300.