The following data is part of a premarket notification filed by Kli with the FDA for Dual Incision Tubal Occlus. Band Appli..
| Device ID | K771961 |
| 510k Number | K771961 |
| Device Name: | DUAL INCISION TUBAL OCCLUS. BAND APPLI. |
| Classification | Laparoscope, Gynecologic (and Accessories) |
| Applicant | KLI 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 | 1977-10-17 |
| Decision Date | 1977-10-25 |