The following data is part of a premarket notification filed by Karl Storz Endoscopy-america, Inc. with the FDA for Cannula, W/sharp Obturator & Veress Need.
| Device ID | K800668 |
| 510k Number | K800668 |
| Device Name: | CANNULA, W/SHARP OBTURATOR & VERESS NEED |
| Classification | Laparoscope, Gynecologic (and Accessories) |
| Applicant | KARL STORZ ENDOSCOPY-AMERICA, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HET |
| CFR Regulation Number | 884.1720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-03-26 |
| Decision Date | 1980-05-08 |