510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K955742Substantially Equivalent

D. Device II

Yousef Daneshvar, Livonia MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K955742 is the FDA 510(k) clearance record for D. DEVICE II, a class II device, cleared for Yousef Daneshvar on under FDA product code DXC (Clamp, Vascular). FDA records list one 510(k) clearance for Yousef Daneshvar. As of , FDA records show no recalls naming K955742.

Clearance record

Decision date
Received
(237 days to decision)
Product code
DXC Clamp, Vascular
Regulation
21 CFR 870.4450
Device class
Class II
Review panel
Cardiovascular
Applicant
Yousef Daneshvar 33433 W. Six Mile Rd., Livonia MI
510(k) summary
Statement
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