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
1959573396
Device Listing 1959573396
Listing Summary
#
Listing key
1959573396
Premarket submission
K240463
Device
Slow Wave DS8 (SWDS802)
Applicant
Slow Wave, Inc.
Product code
MQC
Decision date
2024-06-04
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
280854
3017520337
3017520337
Slow Wave, Inc.
1
N
2026-01-01
22111 Tx Hwy 71 W Ste 104 Spicewood TX US 78669