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Ml 830®

FDA UDI

Class II (US FDA UDI)

by Microlight Corporation Of America

Identity

Trade Name
ML 830® FDA UDI
Generic Name
Musculoskeletal/physical therapy laser, home-use FDA UDI
Device Name
SL Single Probe FDA UDI
Model / Reference
ML-830-07-002 FDA UDI
Description
SL Single Probe FDA UDI

Identifiers

Catalog Number
ML-830-07-002 FDA UDI
Primary DI / UDI-DI
00859626006275 FDA UDI
510(k) Number
K080786 FDA UDI
FDA Product Code
ILY FDA UDI
GMDN Term
Musculoskeletal/physical therapy laser, home-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Musculoskeletal/physical therapy laser, home-use

Ml 830® by Microlight Corporation Of America — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Musculoskeletal/physical therapy laser, home-use.

Cleared under the same submission

K080786 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Microlight Corporation Of America

Sources (1)

  • FDA UDI 99a0af37-dab3-4ca7-a69a-f163058eb702 36 fields · synced May 30, 2026