The following data is part of a premarket notification filed by Ge Medical Systems Ultrasound And Primary Care Diagnostics, with the FDA for Logiq F8 Expert, Logiq F8, Logiq F6.
| Device ID | K160277 |
| 510k Number | K160277 |
| Device Name: | LOGIQ F8 Expert, LOGIQ F8, LOGIQ F6 |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Applicant | GE Medical Systems Ultrasound And Primary Care Diagnostics, 9900 W. Innovation Drive Wauwatosa, WI 53226 |
| Contact | Tracey Ortiz |
| Correspondent | Tracey Ortiz GE Medical Systems Ultrasound And Primary Care Diagnostics, 9900 W. Innovation Drive Wauwatosa, WI 53226 |
| Product Code | IYN |
| Subsequent Product Code | ITX |
| Subsequent Product Code | IYO |
| CFR Regulation Number | 892.1550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-02-02 |
| Decision Date | 2016-03-25 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00840682117210 | K160277 | 000 |
| 00840682116831 | K160277 | 000 |
| 00840682108041 | K160277 | 000 |
| 00840682104975 | K160277 | 000 |
| 00840682103695 | K160277 | 000 |
| 00840682103657 | K160277 | 000 |
| 00840682103565 | K160277 | 000 |