Model PMT850
510(k) K070931
Model PMT850 is a Class II device made by Promedtek, Inc., cleared under FDA 510(k) K070931 on 24 May 2007, active as of 9 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK070931 | Date24 May 2007 | StatusActive |
Official records
- FDA 510(k) database K070931
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- ILX
- Device class
- Class II
- Regulation
- 21 CFR Part 890.5290
- Advisory committee
- Physical Medicine
- FDA decision
- SESE Substantially Equivalent
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