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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Electrosurgical, Cutting & Coagulation & Accessories
510(k) Number K932392
Device Name PHX TECHNOLOGIES CORP ELECTROSURGICAL PROBES
Applicant
Phx Technologies Corp.
1019 Ridgecrest Cir.
Denton,  TX  76205
Applicant Contact JAMES F CHAPEL
Correspondent
Phx Technologies Corp.
1019 Ridgecrest Cir.
Denton,  TX  76205
Correspondent Contact JAMES F CHAPEL
Regulation Number878.4400
Classification Product Code
GEI  
Subsequent Product Code
GCJ  
Date Received05/18/1993
Decision Date 11/22/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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