The following data is part of a premarket notification filed by Ipco Corp. with the FDA for Tube, Sterile Non-conductive Connecting.
| Device ID | K760203 |
| 510k Number | K760203 |
| Device Name: | TUBE, STERILE NON-CONDUCTIVE CONNECTING |
| Classification | Connector, Catheter |
| Applicant | IPCO CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GCD |
| CFR Regulation Number | 878.4200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-07-08 |
| Decision Date | 1976-07-19 |