The following data is part of a premarket notification filed by Lifequest Endoscopic Technologies, Inc. with the FDA for Lquet Cannula/trocar System.
| Device ID | K974139 |
| 510k Number | K974139 |
| Device Name: | LQUET CANNULA/TROCAR SYSTEM |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | LIFEQUEST ENDOSCOPIC TECHNOLOGIES, INC. 12961 PARK CENTRAL, SUITE 1300 San Antonio, TX 78216 |
| Contact | Jeffrey Scott |
| Correspondent | Jeffrey Scott LIFEQUEST ENDOSCOPIC TECHNOLOGIES, INC. 12961 PARK CENTRAL, SUITE 1300 San Antonio, TX 78216 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-11-03 |
| Decision Date | 1998-01-28 |
| Summary: | summary |