The following data is part of a premarket notification filed by Medeon Biodesign, Inc with the FDA for Laparoscope Lens Shield Device.
Device ID | K151117 |
510k Number | K151117 |
Device Name: | Laparoscope Lens Shield Device |
Classification | Laparoscope, General & Plastic Surgery |
Applicant | Medeon Biodesign, Inc 7F, 116 Hougang St Taipei, TW 11170 |
Contact | Greta Chang |
Correspondent | Greta Chang Lin & Associate, LLC 9223 Cambridge Manor Court Potomac, MD 20854 |
Product Code | GCJ |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-04-27 |
Decision Date | 2015-08-20 |