The following data is part of a premarket notification filed by Phx Technologies Corp. with the FDA for Phx Technologies Corp Electrosurgical Probes.
| Device ID | K932392 |
| 510k Number | K932392 |
| Device Name: | PHX TECHNOLOGIES CORP ELECTROSURGICAL PROBES |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | PHX TECHNOLOGIES CORP. 1019 RIDGECREST CIRCLE Denton, TX 76205 |
| Contact | James F Chapel |
| Correspondent | James F Chapel PHX TECHNOLOGIES CORP. 1019 RIDGECREST CIRCLE Denton, TX 76205 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-05-18 |
| Decision Date | 1993-11-22 |