Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K980038
Device Classification Name
Latex Patient Examination Glove
More FDA Info for this Device
510(K) Number
K980038
Device Name
Latex Patient Examination Glove
Applicant
SRI JOHANI SDN. BHD.
LOT PT 7178, BALAKONG N/V,
SERI KEMBANGAN
SELANGOR 43300 MY
Other 510(k) Applications for this Company
Contact
LIM L AIK
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
01/05/1998
Decision Date
02/09/1998
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
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact