Diagnostix™ 9000TRP
by American Diagnostic Corporation
Diagnostix™ 9000TRP is a Class II device made by American Diagnostic Corporation, cleared under FDA 510(k) K070750 on 2 May 2007 and listed in FDA GUDID since 21 Sep 2016 (UDI-DI 00634782065003), active as of 23 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 | Number00634782065003 | Date21 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK070750 | Date2 May 2007 | StatusActive |
Official records
- AccessGUDID record 00634782065003
- FDA 510(k) database K070750
Across registries
- FDA 510(k) K070750 decided 2 May 2007 Active
- FDA GUDID UDI-DI 00634782065003 listed 21 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K070750
- Listed FDA GUDID 00634782065003
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Diagnostix™
- Generic name
- Automatic-inflation electronic sphygmomanometer, non-portable
- Model / Ref / Catalog
- 9000TRP
- Primary DI / UDI-DI
- 00634782065003
- 510(k) Number
- FDA product code
- DXN
- GMDN term
- Automatic-inflation electronic sphygmomanometer, non-portable
- Device class
- Class II
- Regulation number
- 870.1130
- GUDID distribution status
- In Commercial Distribution
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