510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K093813Substantially Equivalent

Occlusin 500 Artificial Embolization Device

Imbiotechnologies Ltd, North Attleboro MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K093813 is the FDA 510(k) clearance record for OCCLUSIN 500 ARTIFICIAL EMBOLIZATION DEVICE, a class II device, cleared for Imbiotechnologies on under FDA product code KRD (Device, Vascular, For Promoting Embolization). FDA records list one 510(k) clearance for Imbiotechnologies. As of , FDA records show no recalls naming K093813.

Clearance record

Decision date
Received
(150 days to decision)
Product code
KRD Device, Vascular, For Promoting Embolization
Regulation
21 CFR 870.3300
Device class
Class II
Review panel
Cardiovascular
Applicant
Imbiotechnologies 49 Plain St., North Attleboro MA
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