The following data is part of a premarket notification filed by Phx Technologies Corp. with the FDA for Phx Technologies Corp, Sponge Grasper Device.
| Device ID | K934025 |
| 510k Number | K934025 |
| Device Name: | PHX TECHNOLOGIES CORP, SPONGE GRASPER DEVICE |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | PHX TECHNOLOGIES CORP. POST OFFICE BOX 1059 Lewisville, TX 75067 |
| Contact | James F Chapel |
| Correspondent | James F Chapel PHX TECHNOLOGIES CORP. POST OFFICE BOX 1059 Lewisville, TX 75067 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-08-17 |
| Decision Date | 1993-12-17 |