Iradimed 1834SA-10
Iradimed 1834SA-10 is a Class II device made by Iradimed Corporation, cleared under FDA 510(k) K172200 on 25 Oct 2017 and listed in FDA GUDID since 15 Apr 2021 (UDI-DI 00856038001294), 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 | Number00856038001294 | Date15 Apr 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK172200 | Date25 Oct 2017 | StatusActive |
Official records
- AccessGUDID record 00856038001294
- FDA 510(k) database K172200
Across registries
- FDA 510(k) K172200 decided 25 Oct 2017 Active
- FDA GUDID UDI-DI 00856038001294 listed 15 Apr 2021 Listed
Timeline
- Cleared FDA 510(k) K172200
- Listed FDA GUDID 00856038001294
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Iradimed
- Generic name
- Blood pressure cuff, single-use
- Model / Ref / Catalog
- 1834SA-10
- Primary DI / UDI-DI
- 00856038001294
- 510(k) Number
- FDA product code
- MWI
- GMDN term
- Blood pressure cuff, single-use
- Device class
- Class II
- Regulation number
- 870.2300
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
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