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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Latex Patient Examination Glove
510(k) Number K891940
Device Name PATIENT EXAM GLOVES (MFG. MOSS POINT GLOVE CO.)
Applicant
Tillotson Corp.
59 Waters Ave.
Everett,  MA  02149
Applicant Contact IMOGENE TIBBETTS
Correspondent
Tillotson Corp.
59 Waters Ave.
Everett,  MA  02149
Correspondent Contact IMOGENE TIBBETTS
Regulation Number880.6250
Classification Product Code
LYY  
Date Received03/28/1989
Decision Date 07/14/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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