Home › METTLER ELECTRONICS CORP. › Applicator 7310
Applicator 7310
METTLER ELECTRONICS CORP. · Model 7310 · UDI-DI 00816864020746
1
510(k) clearances
235
Adverse events (2 deaths)
2
Recalls
24
Facilities
Description
716, 730, 992, 994 applicator (10 cm sq./ 1 MHz)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-02-28 | Chattanooga Corp Inc | Device may fail to administer therapy during use. |
| 2008-02-28 | Chattanooga Corp Inc | Device may fail to administer therapy during use. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
