The following data is part of a premarket notification filed by Medsys, S.a. with the FDA for Lapman Laparoscope Manipulator System And Accessories, Model 900-001.
Device ID | K023735 |
510k Number | K023735 |
Device Name: | LAPMAN LAPAROSCOPE MANIPULATOR SYSTEM AND ACCESSORIES, MODEL 900-001 |
Classification | Laparoscope, General & Plastic Surgery |
Applicant | MEDSYS, S.A. 13723 DANA LN. EAST Puyallup, WA 98373 |
Contact | Jeff Morgan |
Correspondent | Jeff Morgan MEDSYS, S.A. 13723 DANA LN. EAST Puyallup, WA 98373 |
Product Code | GCJ |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-11-07 |
Decision Date | 2003-08-07 |
Summary: | summary |