The following data is part of a premarket notification filed by Shangdong Huamei Technology Co., Ltd. with the FDA for Photodynamic Therapy (pdt) Equipment.
| Device ID | K200751 |
| 510k Number | K200751 |
| Device Name: | Photodynamic Therapy (PDT) Equipment |
| Classification | Powered Laser Surgical Instrument |
| Applicant | Shangdong Huamei Technology Co., Ltd. No. 588, Changning Street, High-tech District Weifang, CN 261205 |
| Contact | Xu Qinghua |
| Correspondent | Ray Wang Beijing Believe-Med Technology Service Co., Ltd. Rm. 912, Building #15, XiYueHui, No.5, YiHe North Rd., FangShan District Beijing, CN 102401 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2020-03-23 |
| Decision Date | 2020-05-21 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 06973512860315 | K200751 | 000 |
| 06973512860346 | K200751 | 000 |
| 06973512860339 | K200751 | 000 |
| 06973512860322 | K200751 | 000 |