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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name motor, surgical instrument, ac-powered
510(k) Number K843519
Device Name MINUTEMAN CO2 MICROSURG LASER GEN SURG
Applicant
AMERICAN SURGICAL LASER, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Applicant Contact RICHARD W TUCKER
Correspondent
AMERICAN SURGICAL LASER, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent Contact RICHARD W TUCKER
Regulation Number878.4820
Classification Product Code
GEY  
Date Received09/05/1984
Decision Date 12/07/1984
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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