FDA 510(k), K891939, NON STERILE EXAM GLOVES ( TILLOTSON RUBBER CO.)

FDA 510(k), K891939, NON STERILE EXAM GLOVES ( TILLOTSON RUBBER CO.)

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510(K) Number: K891939
Device Name: NON STERILE EXAM GLOVES ( TILLOTSON RUBBER CO.)
Manufacturer: IMOGENE TIBBETTS
Device Classification Name: Latex Patient Examination Glove
Regulation Number: LYY
Classification Product Code: 03/28/1989
Date Received: 07/14/1989
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital

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