Monitoring Kit, Central Venous Pressure
by Argon Medical Corp. 510(k)
Active
510(k) K770290
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK770290 | Date15 Mar 1977 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- DQO
- Device Class
- Class II
- Regulation
- 21 CFR Part 870.1200
- Advisory Committee
- Cardiovascular
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 1 Oct 2026
This device is a monitoring kit for central venous pressure, designed for accurate and reliable hemodynamic monitoring. It provides precise pressure transmission and dependable connectivity across a range of clinical applications.
The kit is supplied in multiple lengths and connector configurations to support both standard and specialized monitoring setups. It received FDA 510(k) clearance (K770290) on March 15, 1977, under product code DQO, and is manufactured by Argon Medical Corp. in McHenry, Illinois.
Other devices from Argon Medical Corp.
Questions
AI-generated answers, 1 Oct 2026
What is the Monitoring Kit, Central Venous Pressure used for?
This device is designed for accurate and reliable hemodynamic monitoring by providing precise pressure transmission and dependable connectivity in central venous pressure monitoring across various clinical applications.
How is the Monitoring Kit, Central Venous Pressure supplied?
The kit is supplied in multiple lengths and connector configurations to support both standard and specialized monitoring setups, allowing flexibility for different clinical needs.
What regulatory clearance does the Monitoring Kit, Central Venous Pressure have?
The device received FDA 510(k) clearance under number K770290 on March 15, 1977, based on a traditional submission and was found substantially equivalent to a predicate device.