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
K761169Substantially Equivalent

Grant Modif of Debakey Abdom Aorta Clmp

Pilling Co., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K761169 is the FDA 510(k) clearance record for GRANT MODIF OF DEBAKEY ABDOM AORTA CLMP, a class II device, cleared for Pilling Co. on under FDA product code DXC (Clamp, Vascular). FDA records list 40 510(k) clearances for Pilling Co., from to . As of , FDA records show no recalls naming K761169.

Clearance record

Decision date
Received
(8 days to decision)
Product code
DXC Clamp, Vascular
Regulation
21 CFR 870.4450
Device class
Class II
Review panel
Cardiovascular
Applicant
Pilling Co. 803 N. Front St. Suite 3, Mchenry IL
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