Dittmann LD-753
Dittmann LD-753 is a Class II device made by Honsun (Nantong) Co., Ltd, cleared under FDA 510(k) K131463 on 8 Jul 2013 and listed in FDA GUDID since 3 Feb 2018 (UDI-DI 00697038425648), 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 | Number00697038425648 | Date3 Feb 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK131463 | Date8 Jul 2013 | StatusActive |
Official records
- AccessGUDID record 00697038425648
- FDA 510(k) database K131463
Across registries
- FDA 510(k) K131463 decided 8 Jul 2013 Active
- FDA GUDID UDI-DI 00697038425648 listed 3 Feb 2018 Listed
Timeline
- Cleared FDA 510(k) K131463
- Listed FDA GUDID 00697038425648
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Dittmann
- Generic name
- Automatic-inflation electronic sphygmomanometer, portable, finger
- Model / reference
- LD-753
- Primary DI / UDI-DI
- 00697038425648
- 510(k) Number
- FDA product code
- DXN
- GMDN term
- Automatic-inflation electronic sphygmomanometer, portable, finger
- Device class
- Class II
- Regulation number
- 870.1130
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
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