Cav 3.0C Software Program
by Siemens Life Support Systems
510(k) K890932
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK890932 | Date12 Jun 1989 | StatusActive |
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- BZK
- Device Class
- Class II
- Regulation
- 21 CFR Part 868.1850
- Advisory Committee
- Anesthesiology
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 27 Sep 2026
The Cav 3.0c Software Program is a spirometer monitoring software, classified as a class 2 device. It is used for monitoring purposes, with or without an alarm. The device falls under the medical specialty of anesthesiology.
The software program is supplied as a traditional clearance type, with a regulation number of 868.1850. It has been authorized with an FDA 510K clearance, with a decision description of substantially equivalent. The device has a product code of BZK and is associated with the K number K890932.
Other devices from Siemens Life Support Systems
Questions
AI-generated answers, 27 Sep 2026
What is the Cav 3.0c Software Program used for?
The Cav 3.0c Software Program is used for monitoring purposes, with or without an alarm, in the medical specialty of anesthesiology.
What type of clearance does the Cav 3.0c Software Program have?
The Cav 3.0c Software Program has been authorized with an FDA 510K clearance, with a decision description of substantially equivalent.
What is the product code of the Cav 3.0c Software Program?
The product code of the Cav 3.0c Software Program is BZK, and it is associated with the K number K890932.
What is the regulation number of the Cav 3.0c Software Program?
The regulation number of the Cav 3.0c Software Program is 868.1850.