The following data is part of a premarket notification filed by Pioneering Technologies, Inc. with the FDA for Pti Intra-art Internal Mammary Artery Cannula Kit.
| Device ID | K894684 |
| 510k Number | K894684 |
| Device Name: | PTI INTRA-ART INTERNAL MAMMARY ARTERY CANNULA KIT |
| Classification | Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass |
| Applicant | PIONEERING TECHNOLOGIES, INC. 3900 YOUNGFIELD ST. Wheat Ridge, CO 80033 |
| Contact | Wright,phd |
| Correspondent | Wright,phd PIONEERING TECHNOLOGIES, INC. 3900 YOUNGFIELD ST. Wheat Ridge, CO 80033 |
| Product Code | DWF |
| CFR Regulation Number | 870.4210 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-07-25 |
| Decision Date | 1989-10-17 |