FDA UDI In Commercial Distribution 🇺🇸 United States

JLK-ICH

DI: 08800066200589 · Model: V1.0.0.0 · JLK, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
JLK-ICH
Primary DI
08800066200589
Version / Model
V1.0.0.0
Company Name
JLK, Inc.
Labeler DUNS
689695319
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
c5679774-fe9c-4f95-886a-2c001c4e02ee

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
QAS Radiological Computer-Assisted Triage And Notification Software

GMDN Terms

Code Name
57812 Radiology DICOM image processing application software

Identifiers

Type ID
Primary 08800066200589

Premarket Submissions

Submission Number Supplement Number
K243363 000