Bio Protech MaxEMS 1k
Bio Protech MaxEMS 1k is a medical device (FDA Class II; FDA product code IPF, Stimulator, Muscle, Powered) made by Bio Protech USA, Inc., cleared under FDA 510(k) K091248 on 30 Nov 2009 and listed in FDA GUDID since 16 Jun 2016 (UDI-DI 00817120020074), 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 | Number00817120020074 | Date16 Jun 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK091248 | Date30 Nov 2009 | StatusActive |
Official records
- AccessGUDID record 00817120020074
- FDA 510(k) database K091248
Across registries
- FDA 510(k) K091248 decided 30 Nov 2009 Active
- FDA GUDID UDI-DI 00817120020074 listed 16 Jun 2016 Listed
Timeline
- Cleared FDA 510(k) K091248
- Listed FDA GUDID 00817120020074
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Bio Protech
- Generic name
- Physical therapy transcutaneous neuromuscular electrical stimulation system
- Model / reference
- MaxEMS 1k
- Primary DI / UDI-DI
- 00817120020074
- 510(k) Number
- FDA product code
- IPF
- GMDN term
- Physical therapy transcutaneous neuromuscular electrical stimulation system
- Device class
- Class II
- Regulation number
- 890.5850
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Physical therapy transcutaneous neuromuscular electrical stimulation system.