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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K861360
Device Name MANIQUICK PEDICURE & MANICURE SET
Applicant
Quicklime Maniquick
2738 Ct.
Switzerland,  CH
Applicant Contact MARCHAND S.A
Correspondent
Quicklime Maniquick
2738 Ct.
Switzerland,  CH
Correspondent Contact MARCHAND S.A
Date Received04/10/1986
Decision Date 07/21/1986
Decision Substantially Equivalent (SESE)
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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