FDA UDI In Commercial Distribution 🇺🇸 United States

WAVi Scan Kit

DI: B592WK200 · Model: WK200 · WAVI CO.
Product Codes
4
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
WAVi Scan Kit
Primary DI
B592WK200
Version / Model
WK200
Company Name
WAVI CO.
Labeler DUNS
007785282
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-03-25
Public Version
1
Public Version Date
2026-04-02
Public Version Status
New
Public Device Record Key
0c5f7202-917c-43b7-be69-dcb9f63e5fe8

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GWQ Full-Montage Standard Electroencephalograph
OLT Non-Normalizing Quantitative Electroencephalograph Software
GWJ Stimulator, Auditory, Evoked Response
GXY Electrode, Cutaneous

GMDN Terms

Code Name
11467 Electroencephalograph
61020 Analytical non-scalp cutaneous electrode

Identifiers

Type ID
Primary B592WK200

Premarket Submissions

Submission Number Supplement Number
K162460 000
K213900 000