Calcium Electrode 2150
by Medica Corp.
Calcium Electrode 2150 is a Class II device made by Medica Corp., cleared under FDA 510(k) K943091 on 17 Jan 1995 and listed in FDA GUDID since 8 Nov 2018 (UDI-DI 00386100003135), 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 | Number00386100003135 | Date8 Nov 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK943091 | Date17 Jan 1995 | StatusActive |
Official records
- AccessGUDID record 00386100003135
- FDA 510(k) database K943091
Across registries
- FDA 510(k) K943091 decided 17 Jan 1995 Active
- FDA GUDID UDI-DI 00386100003135 listed 8 Nov 2018 Listed
Timeline
- Cleared FDA 510(k) K943091
- Listed FDA GUDID 00386100003135
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Calcium Electrode
- Generic name
- Calcium (Ca2+) electrode IVD
- Model / Ref / Catalog
- 2150
- Primary DI / UDI-DI
- 00386100003135
- 510(k) Number
- FDA product code
- JFP
- GMDN term
- Calcium (Ca2+) electrode IVD
- Device class
- Class II
- Regulation number
- 862.1145
- GUDID distribution status
- In Commercial Distribution
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