Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K212482
Device Classification Name
Latex Patient Examination Glove
More FDA Info for this Device
510(K) Number
K212482
Device Name
Latex Patient Examination Glove
Applicant
Sri Trang Gloves (Thailand) Public Company Limited
10 SOi 10 Phetkasem Road
Hatyai 90110 TH
Other 510(k) Applications for this Company
Contact
Jarinya Jirokjul
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
08/09/2021
Decision Date
08/09/2022
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Statement
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact