510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K892446Substantially Equivalent

Shiley Equipment Support Carts Esc-002 & Escb-02

Shiley, Inc., Irvine CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K892446 is the FDA 510(k) clearance record for SHILEY EQUIPMENT SUPPORT CARTS ESC-002 & ESCB-02, a class II device, cleared for Shiley, Inc. on under FDA product code KRD (Device, Vascular, For Promoting Embolization). FDA records list 174 510(k) clearances for Shiley, Inc., from to . As of , FDA records show no recalls naming K892446.

Clearance record

Decision date
Received
(95 days to decision)
Product code
KRD Device, Vascular, For Promoting Embolization
Regulation
21 CFR 870.3300
Device class
Class II
Review panel
Cardiovascular
Applicant
Shiley, Inc. 17600 Gillette Ave., Irvine CA
Third party review
No

Clearances, product code KRD

Trailing 12 months
7 clearances under product code KRD in the twelve months to October 2026, June 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code KRD, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20260
March 20260
April 20261
May 20260
June 20262
July 20262
August 20260
September 20260
October 20260