Lumecca 515 - Lumecca 515 - INMODE M.D LTD

Duns Number:600417351

Device Description: Lumecca 515

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More Product Details

Catalog Number

AS601863A

Brand Name

Lumecca 515

Version/Model Number

AS601863A

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

K123860

Product Code Details

Product Code

ONF

Product Code Name

Powered Light Based Non-Laser Surgical Instrument With Thermal Effect

Device Record Status

Public Device Record Key

5a74dc38-f282-4a50-9a36-37a9e61794d5

Public Version Date

January 07, 2019

Public Version Number

3

DI Record Publish Date

October 25, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"INMODE M.D LTD" 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. 15