Swan-Ganz Pacing Probe and Catheters +4 more— 510(k) K233983
Substantially EquivalentEdwards Lifesciences
FDA 510(k) clearance K233983 for Swan-Ganz Pacing Probe and Catheters +4 more, Substantially Equivalent on 2024-06-27. Applicant: Edwards Lifesciences. Device class: 2.
Clearance details
- Device name as filed
- Swan-Ganz Pacing Probe and Catheters; Swan-Ganz Bipolar Pacing Catheter (D97120F5); Swan-Ganz Bipolar Pacing Catheter (D97130F5); Swan-Ganz Pacing Thermodilution TD Catheter (D200F7); Chandler Transluminal V-Pacing Probe (D98100)
- Applicant
- Edwards Lifesciences
- Product code
- Code DYG
- Device class
- Class 2
- Regulation
- 21 CFR 870.1240
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
Recent devices under product code DYG
view all- K242451 — HemoSphere Alta Advanced Monitoring Platform (ALTAALL1/ALTCR1/ALTASR1) +2 more
- K233824 — Swan-Ganz catheter
- K231248 — Swan-Ganz Catheters, FloTrac sensors, ClearSight finger cuffs, HemoSphere Advanced Monitoring Platform
- K222117 — Swang-Ganz IQ pulmonary artery catheter
- K193466 — Swan-Ganz Catheters
More clearances from Edwards Lifesciences
view allAdverse events under product code DYG
product code DYG- Death
- 18
- Malfunction
- 1,051
- Other
- 1
- Total
- 1,070
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recalls naming K233983
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K233983.
Data sourced from openFDA. This site is unofficial and independent of the FDA.