FDA UDI In Commercial Distribution 🇺🇸 United States

ML 830®

DI: 00859626006343 · Model: ML-830-07-100 · MICROLIGHT CORPORATION OF AMERICA
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ML 830®
Primary DI
00859626006343
Version / Model
ML-830-07-100
Catalog Number
ML-830-07-100
Company Name
MICROLIGHT CORPORATION OF AMERICA
Labeler DUNS
137829417
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-12
Public Version
2
Public Version Date
2022-12-08
Public Version Status
Update
Public Device Record Key
c0a8cf3a-4ae2-4d31-a09f-3dcae305a3db

Device Description

Smart Laser DP

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
Yes
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
NHN Powered Light Based Non-Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy
ILY Lamp, Infrared, Therapeutic Heating

GMDN Terms

Code Name
60410 Musculoskeletal/physical therapy laser, home-use

Identifiers

Type ID
Primary 00859626006343

Customer Contacts

Phone
7135200668

Premarket Submissions

Submission Number Supplement Number
K010175 000
K080786 000