The following data is part of a premarket notification filed by Innervision, Inc. with the FDA for Innervision Inc. Cannula/trocar,multiple Types.
| Device ID | K940731 |
| 510k Number | K940731 |
| Device Name: | INNERVISION INC. CANNULA/TROCAR,MULTIPLE TYPES |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | INNERVISION, INC. 1755 LYNNFIELD RD. SUITE 190 Memphis, TN 38119 |
| Contact | Frank M Lewis |
| Correspondent | Frank M Lewis INNERVISION, INC. 1755 LYNNFIELD RD. SUITE 190 Memphis, TN 38119 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-02-18 |
| Decision Date | 1994-09-13 |