510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K250079Substantially Equivalent

Ruby XL System

Penumbra Inc., Alameda CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K250079 is the FDA 510(k) clearance record for Ruby XL System, a class II device, cleared for Penumbra, Inc. on under FDA product code KRD (Device, Vascular, For Promoting Embolization). FDA records list 87 510(k) clearances for Penumbra, Inc., from to . As of , FDA records show no recalls naming K250079.

Clearance record

Decision date
Received
(60 days to decision)
Product code
KRD Device, Vascular, For Promoting Embolization
Regulation
21 CFR 870.3300
Device class
Class II
Review panel
Cardiovascular
Applicant
Penumbra, Inc. One Penumbra Pl., Alameda CA
510(k) summary
Summary PDF
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