The following data is part of a premarket notification filed by Lg Electronics with the FDA for 27hj713s.
| Device ID | K170899 |
| 510k Number | K170899 |
| Device Name: | 27HJ713S |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | LG Electronics 222, LG-ro, Cheongho-ri, Jinwi-myeon Pyeongtaek-si, KR 17709 |
| Contact | Jinhwan Jun |
| Correspondent | Jinhwan Jun LG Electronics 222, LG-ro, Cheongho-ri, Jinwi-myeon Pyeongtaek-si, KR 17709 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-03-27 |
| Decision Date | 2017-05-30 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00719192617612 | K170899 | 000 |