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
1606001643
Device Listing 1606001643
Listing Summary
#
Listing key
1606001643
Premarket submission
K150400
Device
Renu Gel
Applicant
Cytophil, Inc.
Product code
MIX
Decision date
2015-04-06
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
201423
2183828
2183828
STERIS Laboratories
1
N
2026-01-01
9303 West Broadway Ave. Brooklyn Park MN US 55445