Thd Slide
by Thd SpA
510(k) K081429
Thd Slide is a Class II device made by Thd SpA, cleared under FDA 510(k) K081429 on 30 Jul 2008, 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 | NumberK081429 | Date30 Jul 2008 | StatusActive |
Official records
- FDA 510(k) database K081429
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- JAF
- Device class
- Class II
- Regulation
- 21 CFR Part 892.1540
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code JAF (Monitor, Ultrasonic, Nonfetal).
- MULTI DOPPLEX, MD-1 by Huntleigh Technology, Inc.
- DOPPLER GUIDED PROCTOSCOPE, MODEL 500H by Multigon Industries, Inc.
- HANDHELD DOPLER/PEN TRANSDUCER 3MHZ by Philips Medical Systems
- BIOSENSOR BIDOP VASCULAR TEST SYSTEM by Biosensor Corp.
- NICOLET VERSALAB by Nicolet Biomedical, Inc.
- THD by G.F. S.R.L.
- FLOSTAT VASCULAR LAB by BIOMEDIX-INC
- R AND D BATTERIES by R & D BATTERIES, INC.
- MINIVASON 9 by Kt Medical, Inc.
- VISTA AVS by Summit Doppler Systems, Inc.