Acculite EndoOcular - LUMENIS INC.

Duns Number:043618763

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More Product Details

Catalog Number

-

Brand Name

Acculite EndoOcular

Version/Model Number

Illum/Sm Plug, 20ga 45°, SMA 906, 200µm

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

May 20, 2019

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

Yes

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

K931784,K931784

Product Code Details

Product Code

HQF

Product Code Name

Laser, Ophthalmic

Device Record Status

Public Device Record Key

e7f67908-b654-453a-8a49-4aea3b3b4afa

Public Version Date

May 21, 2019

Public Version Number

4

DI Record Publish Date

September 25, 2016

Additional Identifiers

Package DI Number

17290109140800

Quantity per Package

10

Contains DI Package

07290109140803

Package Discontinue Date

May 20, 2019

Package Status

Not in Commercial Distribution

Package Type

-

"LUMENIS INC." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 48