Baxter-022
by Pro Medical Supplies, Inc. 3 variants
Baxter-022 is a Class II device made by Pro Medical Supplies, Inc., cleared under FDA 510(k) K132998 on 20 Dec 2013 and listed in FDA GUDID since 24 Aug 2016 (UDI-DI 10185098000846), 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 | Number10185098000846 | Date24 Aug 2016 | StatusListed |
| United States | FDA 510(k) | NumberK132998 | Date20 Dec 2013 | StatusActive |
Official records
- AccessGUDID record 10185098000846
- FDA 510(k) database K132998
Across registries
- FDA 510(k) K132998 decided 20 Dec 2013 Active
- FDA GUDID UDI-DI 10185098000846 listed 24 Aug 2016 Listed
Timeline
- Cleared FDA 510(k) K132998
- Listed FDA GUDID 10185098000846
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Baxter
- Generic name
- Transcutaneous electrical stimulation electrode, single-use
- Model / Ref / Catalog
- Baxter-022
- Description
- (400) Baxter Electrodes 2.0"x2.0" Black Foam (100 Pack = 4 Electrodes Per Pack)
- Primary DI / UDI-DI
- 10185098000846
- 510(k) Number
- FDA product code
- GXY
- GMDN term
- Transcutaneous electrical stimulation electrode, single-use
- Device class
- Class II
- Regulation number
- 882.1320
- GUDID distribution status
- In Commercial Distribution
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