510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K974736Substantially Equivalent

Heartport Direct Aortic Return Cannula with Introducer

Heartport, Inc., Redwood City CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K974736 is the FDA 510(k) clearance record for HEARTPORT DIRECT AORTIC RETURN CANNULA WITH INTRODUCER, a class II device, cleared for Heartport, Inc. on under FDA product code DWF (Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass). FDA records list 24 510(k) clearances for Heartport, Inc., from to . As of , FDA records show 5 recalls naming K974736.

Clearance record

Decision date
Received
(208 days to decision)
Product code
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Regulation
21 CFR 870.4210
Device class
Class II
Review panel
Cardiovascular
Applicant
Heartport, Inc. 200 Chesapeake Dr., Redwood City CA
510(k) summary
Summary
Third party review
No

Clearances, product code DWF

Trailing 12 months
6 clearances under product code DWF in the twelve months to October 2026, January 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code DWF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20262
February 20262
March 20261
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260