LightLas 532/810 - The 532/810 Laser System is included laser - LIGHTMED CORPORATION

Duns Number:657731175

Device Description: The 532/810 Laser System is included laser console, laser delivery unit, and ophthalmic po The 532/810 Laser System is included laser console, laser delivery unit, and ophthalmic powered table. There are 3 boxs individually.

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More Product Details

Catalog Number

-

Brand Name

LightLas 532/810

Version/Model Number

ML0012

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K152688

Product Code Details

Product Code

HQF

Product Code Name

Laser, Ophthalmic

Device Record Status

Public Device Record Key

bbab9e5b-e9e9-4393-bb24-7287fe9904b7

Public Version Date

November 10, 2021

Public Version Number

5

DI Record Publish Date

September 23, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"LIGHTMED CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 3
2 A medical device with a moderate to high risk that requires special controls. 45