Fluoro Catheter
by CMT Medical Technologies, Ltd.
510(k) K953950
Fluoro Catheter is a Class II device made by CMT Medical Technologies, Ltd., cleared under FDA 510(k) K953950 on 18 Sep 1995, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK953950 | Date18 Sep 1995 | StatusActive |
Official records
- FDA 510(k) database K953950
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- JAA
- Device class
- Class II
- Regulation
- 21 CFR Part 892.1650
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
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