Thermo Kor-Continuous Pulmonary Artery Thermometer
FDA 510(k) K901281 · Val-Mark Medical, Inc.
510(k) numberK901281
Submission
- Device name
- Thermo Kor-Continuous Pulmonary Artery Thermometer
- Applicant
- Val-Mark Medical, Inc.
West St. Paul, MN, US - Received
- March 19, 1990
- Decision date
- August 28, 1991
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- DRB – Stylet, Catheter
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1380
- Specialty
- Cardiovascular
Other 510(k)s with product code DRB
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K220280 | Arrow Stiffening StyletDRB · Traditional | Arrow International, LLC (A subsidiary of… | 08/30/2022SE |
| K191469 | Biotronik StyletsDRB · Traditional | Biotronik, Inc. | 08/01/2019SE |
| K182660 | GaltTWSDRB · Traditional | Galt Medical Corp. | 05/30/2019SE |
| K170298 | Liberator Beacon Tip Locking StyletDRB · Traditional | Cook Incorporated | 10/18/2017SE |
| K142116 | LLD EzDRB · Special | Spectranetics, Inc. | 08/12/2014SE |
| K090163 | Stylet, Models 4060, 4062, 4064, 4090, 4091 and 4078DRB · Traditional | St Jude Medical | 04/01/2009SE |
| K080924 | Mond Rvot Stylet Models 4140, 4141, 4150, 4151DRB · Traditional | St. Jude Medical, Cardiac Rhythm Management Divisi | 04/30/2008SE |
| K072864 | St. Jude Medical, CPS Duo Left Heart Lead Delivery SystemDRB · Traditional | St. Jude Medical, Cardiac Rhythm Management Divisi | 03/13/2008SE |
| K053019 | Acuity Steerable Stylet AccessoryDRB · Traditional | Guidant Corporation | 03/03/2006SE |
| K052965 | Easytrak 2 Stylet, Models 4826, 4829, 4832.DRB · Traditional | Guidant Corporation | 02/13/2006SE |
Questions and answers
When was Thermo Kor-Continuous Pulmonary Artery Thermometer cleared by the FDA?
Thermo Kor-Continuous Pulmonary Artery Thermometer (K901281) received a 510(k) decision of Substantially Equivalent on August 28, 1991, 527 days after the submission was received.
What is the product code of K901281?
The FDA product code is DRB – Stylet, Catheter, a Class II (moderate risk) device regulated under 21 CFR 870.1380.