The following data is part of a premarket notification filed by Graphic Controls Corp. with the FDA for Life Trace Trans Tip Intrauterine Pressure Catheter.
Device ID | K950498 |
510k Number | K950498 |
Device Name: | LIFE TRACE TRANS TIP INTRAUTERINE PRESSURE CATHETER |
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 | 1995-02-06 |
Decision Date | 1995-07-24 |