510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K880776Substantially Equivalent

7 Fr. Triple Lumen Central Vein Catheteri. System

Medsurg Industries, Inc., Herndon VA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K880776 is the FDA 510(k) clearance record for 7 FR. TRIPLE LUMEN CENTRAL VEIN CATHETERI. SYSTEM, a class II device, cleared for Medsurg Industries, Inc. on under FDA product code DQR (Cannula, Catheter). FDA records list 41 510(k) clearances for Medsurg Industries, Inc., from to . As of , FDA records show no recalls naming K880776.

Clearance record

Decision date
Received
(66 days to decision)
Product code
DQR Cannula, Catheter
Regulation
21 CFR 870.1300
Device class
Class II
Review panel
Cardiovascular
Applicant
Medsurg Industries, Inc. 251 Exchange Pl., Herndon VA
Third party review
No

Clearances, product code DQR

Trailing 12 months

FDA records hold no clearances under product code DQR in the trailing twelve months.

FDA records show no clearances under product code DQR in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DQR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260