The following data is part of a premarket notification filed by Debusk Technology Corp. with the FDA for Trocar And Cannula.
| Device ID | K941250 |
| 510k Number | K941250 |
| Device Name: | TROCAR AND CANNULA |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | DEBUSK TECHNOLOGY CORP. 200 DEBUSK LN. Powell, TN 37849 |
| Contact | Debra F Manning |
| Correspondent | Debra F Manning DEBUSK TECHNOLOGY CORP. 200 DEBUSK LN. Powell, TN 37849 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-03-15 |
| Decision Date | 1994-05-06 |