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
1620988138
Device Listing 1620988138
Listing Summary
#
Listing key
1620988138
Premarket submission
K971722
Device
TRANS VAGINAL NEEDLE GUIDE
Applicant
Protek Medical Products, Inc.
Product code
ITX
Decision date
1997-07-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
292602
8030607
3006509795
Christopher Smith
1
N
2026-01-01
6945 Southbelt Dr SE Caledonia MI US 49316