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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 K891881
Device Name PATIENT EXAMINATION GLOVE (LATEX)
Applicant
Cymun Development Sdn Bhd
179 Main Rd.
31100 Sungei Siput (U)
Perak, Malaysia,  MY
Applicant Contact HOONG MUN
Correspondent
Cymun Development Sdn Bhd
179 Main Rd.
31100 Sungei Siput (U)
Perak, Malaysia,  MY
Correspondent Contact HOONG MUN
Regulation Number880.6250
Classification Product Code
LYY  
Date Received03/28/1989
Decision Date 05/25/1989
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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