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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Pump, Portable, Aspiration (Manual Or Powered)
510(k) Number K821321
Device Name SNYDER DEBRIBEMENT SYSTEM LDP-1
Applicant
SNYDER LABORATORIES, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
SNYDER LABORATORIES, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number878.4780
Classification Product Code
BTA  
Date Received05/04/1982
Decision Date 08/06/1982
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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