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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Suture, Nonabsorbable, Synthetic, Polypropylene
510(k) Number K960209
Device Name CPR HEART PACK
Applicant
CUSTOM PACK RELIABILITY
4207 VINELAND ROAD, M-1
ORLANDO,  FL  32811
Applicant Contact RICHARD L ELLWOOD
Correspondent
CUSTOM PACK RELIABILITY
4207 VINELAND ROAD, M-1
ORLANDO,  FL  32811
Correspondent Contact RICHARD L ELLWOOD
Regulation Number878.5010
Classification Product Code
GAW  
Date Received01/16/1996
Decision Date 04/04/1996
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
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