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FDA 510(k) Application Details - K182383
Device Classification Name
Patient Examination Glove, Specialty
More FDA Info for this Device
510(K) Number
K182383
Device Name
Patient Examination Glove, Specialty
Applicant
YTY Industry (Manjung) Sdn Bhd
Lot 1422-1424, Batu 10 Lekir
Sitiawan 32020 MY
Other 510(k) Applications for this Company
Contact
Punitha Samy
Other 510(k) Applications for this Contact
Regulation Number
880.6250
More FDA Info for this Regulation Number
Classification Product Code
LZC
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/31/2018
Decision Date
03/19/2019
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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