510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K192413Substantially Equivalent

SiteSeal Femoral Compression Device

Ensite Vacular, LLC, Olathe KS / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K192413 is the FDA 510(k) clearance record for SiteSeal Femoral Compression Device, a class II device, cleared for Ensite Vacular, LLC on under FDA product code DXC (Clamp, Vascular). FDA records list one 510(k) clearance for Ensite Vacular, LLC. As of , FDA records show no recalls naming K192413.

Clearance record

Decision date
Received
(209 days to decision)
Product code
DXC Clamp, Vascular
Regulation
21 CFR 870.4450
Device class
Class II
Review panel
Cardiovascular
Applicant
Ensite Vacular, LLC 10900 S. Clay Blair Blvd., Suite 800, Olathe KS
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DXC

Trailing 12 months
6 clearances under product code DXC in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DXC, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20260
April 20261
May 20261
June 20261
July 20261
August 20260
September 20260
October 20260