The following data is part of a premarket notification filed by Advanced Surgical, Inc. with the FDA for Endoscopic Ligation Device, Ligator Handle, Ligator Cartridge.
Device ID | K950126 |
510k Number | K950126 |
Device Name: | ENDOSCOPIC LIGATION DEVICE, LIGATOR HANDLE, LIGATOR CARTRIDGE |
Classification | Laparoscope, General & Plastic Surgery |
Applicant | ADVANCED SURGICAL, INC. 305 COLLEGE RD. EAST Princeton, NJ 08540 |
Contact | Harriet Schwartzman |
Correspondent | Harriet Schwartzman ADVANCED SURGICAL, INC. 305 COLLEGE RD. EAST Princeton, NJ 08540 |
Product Code | GCJ |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-01-12 |
Decision Date | 1995-04-13 |