The following data is part of a premarket notification filed by Graphic Controls Corp. with the FDA for Lifetrace Intrauterine Pressure Catheter Iup 3000.
| Device ID | K950708 |
| 510k Number | K950708 |
| Device Name: | LIFETRACE INTRAUTERINE PRESSURE CATHETER IUP 3000 |
| Classification | Monitor, Pressure, Intrauterine |
| Applicant | GRAPHIC CONTROLS CORP. PO BOX 1274 189 VAN RENSSELAER STREET Buffalo, NY 14240 |
| Contact | Ignaty Gusakov |
| Correspondent | Ignaty Gusakov GRAPHIC CONTROLS CORP. PO BOX 1274 189 VAN RENSSELAER STREET Buffalo, NY 14240 |
| Product Code | KXO |
| CFR Regulation Number | 884.2700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-02-13 |
| Decision Date | 1995-05-25 |