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FDA 510(k) Application Details - K953462
Device Classification Name
Latex Patient Examination Glove
More FDA Info for this Device
510(K) Number
K953462
Device Name
Latex Patient Examination Glove
Applicant
PT. IRAMA DINAMIKA LATEX
JL. KAPTEN PATTIMURA NO.
MEDAN 20153 ID
Other 510(k) Applications for this Company
Contact
ANIL TANEJA
Other 510(k) Applications for this Contact
Regulation Number
880.6250
More FDA Info for this Regulation Number
Classification Product Code
LYY
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
07/24/1995
Decision Date
01/04/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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