FDA UDI In Commercial Distribution 🇺🇸 United States

VivoSight

DI: 05060507260005 · Model: VivoSight · MICHELSON DIAGNOSTICS LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VivoSight
Primary DI
05060507260005
Version / Model
VivoSight
Company Name
MICHELSON DIAGNOSTICS LTD
Labeler DUNS
349363346
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-14
Public Version
5
Public Version Date
2023-11-10
Public Version Status
Update
Public Device Record Key
51ac505b-901f-4fb0-a934-7998f6295735

Device Description

The VivoSight Topical OCT system is indicated for use in the two-dimensional, cross-sectional, real-time imaging of external tissues of the human body. This indicated use allows imaging of tissue microstructure, including skin, to aid trained and competent clinicians in their assessment of a patient's clinical conditions.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
Yes
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
NQQ System, Imaging, Optical Coherence Tomography (Oct)

GMDN Terms

Code Name
58074 Dermatological optical coherence tomography system

Identifiers

Type ID
Primary 05060507260005

Premarket Submissions

Submission Number Supplement Number
K093520 000