Cadd 21-6300-02
Cadd 21-6300-02 is a Class II device made by ICU Medical, Inc., cleared under FDA 510(k) K982839 on 2 Nov 1998 and listed in FDA GUDID since 13 Oct 2016 (UDI-DI 10610586019357), 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 | Number10610586019357 | Date13 Oct 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK982839 | Date2 Nov 1998 | StatusActive |
Official records
- AccessGUDID record 10610586019357
- FDA 510(k) database K982839
Across registries
- FDA 510(k) K982839 decided 2 Nov 1998 Active
- FDA GUDID UDI-DI 10610586019357 listed 13 Oct 2016 Listed
Timeline
- Cleared FDA 510(k) K982839
- Listed FDA GUDID 10610586019357
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Cadd
- Generic name
- Bedside infusion pump, single-channel
- Model / reference
- 21-6300-02
- Primary DI / UDI-DI
- 10610586019357
- 510(k) Number
- FDA product code
- MEA
- GMDN term
- Bedside infusion pump, single-channel
- Device class
- Class II
- Regulation number
- 880.5725
- GUDID distribution status
- In Commercial Distribution
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