FDA UDI In Commercial Distribution 🇺🇸 United States

K-Scan Evolution

DI: B970KE10 · Model: K-Scan Joint Pressure Measurement System · Tekscan, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
K-Scan Evolution
Primary DI
B970KE10
Version / Model
K-Scan Joint Pressure Measurement System
Catalog Number
KE1
Company Name
Tekscan, Inc.
Labeler DUNS
178180246
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-11-03
Public Version
2
Public Version Date
2020-11-19
Public Version Status
Update
Public Device Record Key
fe535bed-2702-41de-9b7d-828b2713bdb9

Device Description

Includes 1 Evolution Handle, I-Scan Software CD with 2 K-Scan Sensor maps, Sensor Carrying Case, System Carrying Case, and System Manual. 1 Day of Training (USA Only). Sensor selection: Choice of up to 5 sensors corresponding to the maps chosen above (value up to $1,000)

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
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JFC System, Pressure Measurement, Intermittent

GMDN Terms

Code Name
43829 Body-surface pressure mapping system

Identifiers

Type ID
Primary B970KE10