Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1144820978
Device Listing 1144820978
Listing Summary
#
Listing key
1144820978
Premarket submission
K052725
Device
PROTECTOR NEEDLE SHEATH PROP
Applicant
Certol International, LLC
Product code
FMI
Decision date
2005-12-28
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
79725
1720499
1720499
CERTOL INTERNATIONAL, LLC
1
N
2020-04-25
6120 E. 58TH AVE. Commerce City CO US 80022