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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name Laparoscope, General & Plastic Surgery
510(k) Number K952900
Device Name THE TULIP COMPANY BRANSON SOFT TISSUE RETRACTOR
Applicant
THE TULIP MFG. CO.
40 WEST BASELINE RD.,
SUITE 120
MESA,  AZ  85210
Applicant Contact RICHARD S HUNTER
Correspondent
THE TULIP MFG. CO.
40 WEST BASELINE RD.,
SUITE 120
MESA,  AZ  85210
Correspondent Contact RICHARD S HUNTER
Regulation Number876.1500
Classification Product Code
GCJ  
Date Received06/23/1995
Decision Date 10/30/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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