The following data is part of a premarket notification filed by Karl Storz Endoskop Gmbh with the FDA for Torcars,cannulae,sheaths,obturators.
| Device ID | K943713 |
| 510k Number | K943713 |
| Device Name: | TORCARS,CANNULAE,SHEATHS,OBTURATORS |
| Classification | Laparoscope, Gynecologic (and Accessories) |
| Applicant | KARL STORZ ENDOSKOP GMBH 600 CORPORATE POINTE Culver City, CA 90230 |
| Contact | Marika Anderson |
| Correspondent | Marika Anderson KARL STORZ ENDOSKOP GMBH 600 CORPORATE POINTE Culver City, CA 90230 |
| Product Code | HET |
| CFR Regulation Number | 884.1720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-08-01 |
| Decision Date | 1995-06-30 |