Cemax Clinicalview Station And/Or Software
by Cemax, Inc.
510(k) K932371
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK932371 | Date18 Feb 1994 | 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- Withdrawn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
- Full name
- Cemax Clinicalview(Tm) Station and/or Software
- 510(k) Number
- FDA Product Code
- LLZ
- Device Class
- Class II
- Regulation
- 21 CFR Part 892.2050
- Advisory Committee
- Radiology
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 28 Sep 2026
The Cemax Clinicalview Station And/Or Software is a Class II X-ray system. It is used in radiology and provides image processing functions for image manipulation, enhancement, or quantification. The device is manufactured by Cemax, Inc.
The Cemax Clinicalview Station And/Or Software has been issued FDA 510K clearance. It is supplied as a station and/or software. The device has a product code of LLZ and was cleared on February 18, 1994, with the k number K932371.
Other devices from Cemax, Inc.
Questions
AI-generated answers, 28 Sep 2026
What is the Cemax Clinicalview Station used for?
The Cemax Clinicalview Station And/Or Software is used in radiology for image manipulation, enhancement, or quantification.
How is the Cemax Clinicalview Station supplied?
The device is supplied as a station and/or software.
What is the regulatory status of the Cemax Clinicalview Station?
The device has been issued FDA 510K clearance, indicating it is substantially equivalent to a predicate device.