Linear Array Transducer Plu-1003ST
by Canon Inc.
Linear Array Transducer Plu-1003ST is a Class II device made by Canon Inc., cleared under FDA 510(k) K173962 on 20 Apr 2018 and listed in FDA GUDID since 1 Mar 2026 (UDI-DI 04987670102745), 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 | GUDID listing | Number04987670102745 | Date1 Mar 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK173962 | Date20 Apr 2018 | StatusActive |
Official records
- AccessGUDID record 04987670102745
- FDA 510(k) database K173962
Across registries
- FDA 510(k) K173962 decided 20 Apr 2018 Active
- FDA GUDID UDI-DI 04987670102745 listed 1 Mar 2026 Listed
Timeline
- Cleared FDA 510(k) K173962
- Listed FDA GUDID 04987670102745
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Linear Array Transducer
- Generic name
- Extracorporeal ultrasound imaging transducer, hand-held
- Model / reference
- PLU-1003ST
- Primary DI / UDI-DI
- 04987670102745
- 510(k) Number
- FDA product code
- ITX
- GMDN term
- Extracorporeal ultrasound imaging transducer, hand-held
- Device class
- Class II
- Regulation number
- 892.1570
- GUDID distribution status
- In Commercial Distribution
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