Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by KENNY H.N. LIEW
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990499
02/17/1999
PREPOWDERED NITRILE EXAMINATION GLOVES
FLEXITECH SDN. BHD.
K990502
02/17/1999
PREPOWDERED LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (100 MICROGRAMS OR LESS)
FLEXITECH SDN. BHD.
K990495
02/17/1999
POWDER FREE NITRILE EXAMINATION GLOVES
FLEXITECH SDN. BHD.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact