The following data is part of a premarket notification filed by Ge Healthcare with the FDA for Logiq S8.
| Device ID | K170445 |
| 510k Number | K170445 |
| Device Name: | LOGIQ S8 |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Applicant | GE Healthcare 9900 Innovation Dr. Wauwatosa, WI 53226 |
| Contact | Bryan Behn |
| Correspondent | Bryan Behn GE Healthcare 9900 Innovation Dr. 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 | 2017-02-14 |
| Decision Date | 2017-04-11 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00840682144254 | K170445 | 000 |
| 00840682144247 | K170445 | 000 |
| 00840682142793 | K170445 | 000 |
| 00840682122979 | K170445 | 000 |
| 00840682122962 | K170445 | 000 |