The following data is part of a premarket notification filed by Lilium Otsuka Co., Ltd. with the FDA for Lilium A-200e.
| Device ID | K170046 |
| 510k Number | K170046 |
| Device Name: | Lilium A-200E |
| Classification | System, Imaging, Pulsed Echo, Ultrasonic |
| Applicant | Lilium Otsuka Co., Ltd. 4-12-6, Chiyoda, Chuo-ku Sagamihara City, JP 252-0237 |
| Contact | Hiroaki Takahashi |
| Correspondent | Kathryn Coressel Emergo Global Consulting, LLC 2500 Bee Cave Road, Building 1, Suite 300 Austin, TX 78746 |
| Product Code | IYO |
| CFR Regulation Number | 892.1560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-01-05 |
| Decision Date | 2017-12-07 |
| Summary: | summary |