510(k) K092140 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
GE VIVID I DIAGNOSTIC ULTRASOUND, GE VIVID Q DIAGNOSTIC ULTRASOUND
| Applicant | Ge Medical Systems Israel, Ultrasound, Ltd., Waukesha WI, US |
| Decision | Substantially Equivalent, Aug 21, 2009 |
| Received | Jul 15, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K092140
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Dec 22, 2022 | GE Medical Systems, LLC Vivid i ultrasound. Marketed under the following 510(k) numbers: K033139, K061525, K082374, K092140, K102388, K121062).
Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pe Open, Classified |
ITX | None listed |
| Dec 22, 2022 | GE Medical Systems, LLC Vivid q ultrasound.
Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult a Open, Classified |
ITX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.