Applicator 7513
Applicator 7513 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 00816864020630), 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 | Number00816864020630 | Date15 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK984142 | Date9 Feb 1999 | StatusActive |
Official records
- AccessGUDID record 00816864020630
- FDA 510(k) database K984142
Across registries
- FDA 510(k) K984142 decided 9 Feb 1999 Active
- FDA GUDID UDI-DI 00816864020630 listed 15 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K984142
- Listed FDA GUDID 00816864020630
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- Withdrawn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
- 7513
- Primary DI / UDI-DI
- 00816864020630
- 510(k) Number
- FDA product code
- GZJ, IPF, LIH
- GMDN term
- Physical therapy ultrasound system applicator, hand-held
- Device class
- Class II
- Regulation number
- 882.5890, 890.5850
- GUDID distribution status
- In Commercial Distribution
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