FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BARD CATH LAB THERMODILUTION CATHETER
K Number: K893474
·
Decision Sep 5, 1989
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
98
Applicant Total
645
Review Days
124
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- BARD CATH LAB THERMODILUTION CATHETER
- K Number
- K893474
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1240
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- C.R. Bard, Inc.
- Date Received
- May 4, 1989
- Decision Date
- September 5, 1989
- Product Code
- DYG
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| DYG | Catheter, Flow Directed | FDA class 2 | Cardiovascular |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (DYG), ordered by most recent decision date.
HemoSphere Alta Advanced Monitoring Platform (ALTAALL1/ALTCR1/ALTASR1); HemoSphere Alta- monitor pressure cable (HEMAPSC200);Acumen AFM cable- HemoSphere Alta monitor (HEMAFM100)
FDA 510(k)
FDA Class 2
·Cardiovascular
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)
FDA 510(k)
FDA Class 2
·Cardiovascular
Swan-Ganz catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
Swan-Ganz Catheters, FloTrac sensors, ClearSight finger cuffs, HemoSphere Advanced Monitoring Platform
FDA 510(k)
FDA Class 2
·Cardiovascular
Swang-Ganz IQ pulmonary artery catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
Swan-Ganz Catheters
FDA 510(k)
FDA Class 2
·Cardiovascular
Other Clearances by C.R. Bard, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K254076 | BD Touchless Plus Unisex Pre-Lubricated Urethral Catheter Kit | May 29, 2026 | Unknown |
| K252971 | Elyra Thulium Fiber Laser System and Elyra Plus Thulium Fiber Laser System (Laser, Fibers, and Accessories) | Mar 17, 2026 | Substantially Equivalent |
| K251864 | Rubber Utility Catheter | Feb 23, 2026 | Substantially Equivalent |
| K251186 | Bard® Temporary Pacing Electrode Catheter Needle / Cannula (Introducer) | May 15, 2025 | Substantially Equivalent |
| K241334 | Semi-Floating Temporary Pacing Electrode Catheter, Bipolar, Stainless Steel Electrodes, 115 cm, 4Fr. (006221P); Semi-Floating Temporary Pacing Electrode Catheter, Bipolar, Stainless Steel Electrodes, 115 cm, 5Fr. (006225P); Semi-Floating Temporary Pacing Electrode Catheter, Bipolar, Stainless Steel Electrodes, 125 cm, 6Fr. (006241P); Semi-Floating Temporary Pacing Electrode Catheter, Bipolar, Stainless Steel Electrodes, 125 cm, 7Fr. (006242P); NBIH Temporary Pacing Electrode Catheter, | Jan 31, 2025 | Substantially Equivalent |
| K230356 | Aspirex Thrombectomy System | Mar 31, 2023 | Substantially Equivalent |
| K223177 | Highlander 014 PTA Balloon Dilatation Catheter | Jan 20, 2023 | Substantially Equivalent |
| K222793 | WavelinQ Generator | Oct 17, 2022 | Substantially Equivalent |
| K220270 | Aspirex Thrombectomy System | Jun 21, 2022 | Substantially Equivalent |
| K213203 | Provena(TM) Midline Catheter | May 13, 2022 | Substantially Equivalent |