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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 K955501
Device Name THE TULIP MONO POLAR ROTATABLE ALLIGATOR FORCEP
Applicant
The Tulip Mfg. Co.
40 W. Baseline Rd.,
Suite 120
Mesa,  AZ  85210
Applicant Contact RICHARD S HUNTER
Correspondent
The Tulip Mfg. Co.
40 W. Baseline Rd.,
Suite 120
Mesa,  AZ  85210
Correspondent Contact RICHARD S HUNTER
Regulation Number878.4400
Classification Product Code
GEI  
Date Received12/01/1995
Decision Date 01/17/1996
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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