PHX TECHNOLOGIES CORP, SPONGE GRASPER DEVICE

Laparoscope, General & Plastic Surgery

PHX TECHNOLOGIES CORP.

The following data is part of a premarket notification filed by Phx Technologies Corp. with the FDA for Phx Technologies Corp, Sponge Grasper Device.

Pre-market Notification Details

Device IDK934025
510k NumberK934025
Device Name:PHX TECHNOLOGIES CORP, SPONGE GRASPER DEVICE
ClassificationLaparoscope, General & Plastic Surgery
Applicant PHX TECHNOLOGIES CORP. POST OFFICE BOX 1059 Lewisville,  TX  75067
ContactJames F Chapel
CorrespondentJames F Chapel
PHX TECHNOLOGIES CORP. POST OFFICE BOX 1059 Lewisville,  TX  75067
Product CodeGCJ  
CFR Regulation Number876.1500 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1993-08-17
Decision Date1993-12-17

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