Applicator 9402
Applicator 9402 is a Class II device made by Mettler Electronics Corp., cleared under FDA 510(k) K071137 on 1 Aug 2007 and listed in FDA GUDID since 15 Sep 2016 (UDI-DI 00816864020678), active as of 8 Jun 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 | Number00816864020678 | Date15 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK071137 | Date1 Aug 2007 | StatusActive |
Official records
- AccessGUDID record 00816864020678
- FDA 510(k) database K071137
Across registries
- FDA 510(k) K071137 decided 1 Aug 2007 Active
- FDA GUDID UDI-DI 00816864020678 listed 15 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K071137
- Listed FDA GUDID 00816864020678
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Physical therapy ultrasound system applicator, hand-held
- Model / Ref / Catalog
- 9402
- Primary DI / UDI-DI
- 00816864020678
- 510(k) Number
- FDA product code
- GZJ, IMG, LIH
- GMDN term
- Physical therapy ultrasound system applicator, hand-held
- Device class
- Class II
- Regulation number
- 882.5890, 890.5860
- GUDID distribution status
- In Commercial Distribution
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