Applicator 7305
Applicator 7305 is a Class II device made by Mettler Electronics Corp., cleared under FDA 510(k) K934845 on 21 Jan 1994 and listed in FDA GUDID since 15 Sep 2016 (UDI-DI 00816864020739), active as of 21 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 | Number00816864020739 | Date15 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK934845 | Date21 Jan 1994 | StatusActive |
Official records
- AccessGUDID record 00816864020739
- FDA 510(k) database K934845
Across registries
- FDA 510(k) K934845 decided 21 Jan 1994 Active
- FDA GUDID UDI-DI 00816864020739 listed 15 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K934845
- Listed FDA GUDID 00816864020739
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- Withdrawn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
- 7305
- Primary DI / UDI-DI
- 00816864020739
- 510(k) Number
- FDA product code
- IMG
- GMDN term
- Physical therapy ultrasound system applicator, hand-held
- Device class
- Class II
- Regulation number
- 890.5860
- GUDID distribution status
- In Commercial Distribution
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