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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name condom
510(k) Number K993735
Device Name DOUBLE SPRINGERS
Applicant
MEDTECH PRODUCTS LTD.
S-59 20TH ST., ANNA NAGAR WEST
chennai,  IN 600 040
Applicant Contact a.v.k. reddy
Correspondent
MEDTECH PRODUCTS LTD.
S-59 20TH ST., ANNA NAGAR WEST
chennai,  IN 600 040
Correspondent Contact a.v.k. reddy
Regulation Number884.5300
Classification Product Code
HIS  
Date Received11/04/1999
Decision Date 03/20/2000
Decision substantially equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
summary summary
Type Abbreviated
Reviewed by Third Party No
Combination Product No
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