Sonicator Plus 992, 2 channel ME 992
Sonicator Plus 992, 2 channel ME 992 is a Class II device made by Mettler Electronics Corp., cleared under FDA 510(k) K984142 on 9 Feb 1999 and listed in FDA GUDID since 15 Sep 2016 (UDI-DI 00816864020241), 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 | Number00816864020241 | Date15 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK984142 | Date9 Feb 1999 | StatusActive |
Official records
- AccessGUDID record 00816864020241
- FDA 510(k) database K984142
Across registries
- FDA 510(k) K984142 decided 9 Feb 1999 Active
- FDA GUDID UDI-DI 00816864020241 listed 15 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K984142
- Listed FDA GUDID 00816864020241
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Sonicator Plus 992, 2 channel
- Generic name
- Multi-modality physical therapy system, simultaneous, professional-use
- Model / Ref / Catalog
- ME 992
- Primary DI / UDI-DI
- 00816864020241
- 510(k) Number
- FDA product code
- LIH, IPF, GZJ
- GMDN term
- Multi-modality physical therapy system, simultaneous, professional-use
- Device class
- Class II
- Regulation number
- 882.5890, 890.5850
- GUDID distribution status
- In Commercial Distribution
- Size
- Weight — 10.7 Pound
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