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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Curette, Suction, Endometrial (And Accessories)
510(k) Number K881456
Device Name PIPELLE DE CORNIER ENDOMETRIAL SUCTION CURETTE
Applicant
Laboratoire Ccd C/O Washington Regulatory Services
23 Welisewitz Rd.
Ringoes,  NJ  08551
Applicant Contact RANDOLPH L COOKE
Correspondent
Laboratoire Ccd C/O Washington Regulatory Services
23 Welisewitz Rd.
Ringoes,  NJ  08551
Correspondent Contact RANDOLPH L COOKE
Regulation Number884.1175
Classification Product Code
HHK  
Date Received04/06/1988
Decision Date 10/14/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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