PHX TECHNOLOGIES CORP ELECTROSURGICAL PROBES— 510(k) K932392

Name: FDA 510(k) clearance K932392
Creator: U.S. Food and Drug Administration
Published: 1993-11-22

Substantially Equivalent

Phx Technologies Corp.

FDA 510(k) clearance K932392 for PHX TECHNOLOGIES CORP ELECTROSURGICAL PROBES, Substantially Equivalent on 1993-11-22. Applicant: Phx Technologies Corp.. Device class: 2.

Clearance details

Applicant: Phx Technologies Corp.
Product code: Code GEI
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 1993-05-18
Decision date: 1993-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denton, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GEI

view all

K254185 — Potenza Prime2026-09-11
K262364 — Ellian Enigma RF Device2026-09-02
K253859 — Scarlet Pro (Scarlet Pro)2026-08-27
K252535 — Inno-Switch Laparoscopic Instruments2026-08-25
K261179 — AlphaTriPart - Monopolar MIC Instruments2026-07-22

More clearances from Phx Technologies Corp.

view all

K974327 — WINGED NEEDLE HOLDER1998-01-09
K971123 — STONE EXTRACTOR1997-06-27
K954507 — RETROGRADE KNIFE1995-11-14
K954508 — RETRACTOR1995-11-14
K954509 — PROBE KNIFE1995-11-14

Adverse events under product code GEI

product code GEI

Death: 133
Injury: 7,585
Malfunction: 35,808
Other: 44
Total: 43,570

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.