Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by SUNMAX ENTERPRISE SHANGHAI CO. LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090336
02/10/2009
SUNMAX ENTERPRISE SHANGHAI CO. POWDER FREE BLUE NITRILE PATIENT EXAMINATION GLOVE TESTED WITH CHEMOTHERAPY DRUGS
SUNMAX ENTERPRISE SHANGHAI CO. LTD.
K011717
06/04/2001
SUNMAX BLUE NITRILE POWDERED EXAMINATION GLOVES
SUNMAX ENTERPRISE SHANGHAI CO. LTD.
K011765
06/07/2001
SUNMAX BLUE NITRILE POWDER-FREE EXAMINATION GLOVE
SUNMAX ENTERPRISE SHANGHAI CO. LTD.
K964964
12/11/1996
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
SUNMAX ENTERPRISE SHANGHAI CO. LTD.
K960746
02/23/1996
SUNMAX ENTERPRISE SHANGHAI VINYL POWDERED PATIENT EXAM. GLOVES
SUNMAX ENTERPRISE SHANGHAI CO. LTD.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact