Skytron LLC 4A-PF60-ALU

GUDID 10841736123529

60" Protective frame only, requires 4VB/4CM, Freedom, aluminum construction

SKYTRON LLC

General utility supply system, ceiling-mounted
Primary Device ID10841736123529
NIH Device Record Key3927b187-234a-43f1-b01e-75bd74bca2b1
Commercial Distribution StatusIn Commercial Distribution
Brand NameSkytron LLC
Version Model Number4A-PF60-ALU Freedom
Catalog Number4A-PF60-ALU
Company DUNS078375583
Company NameSKYTRON LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us
Phone800-759-8766
Emailinfo@skytron.us

Device Identifiers

Device Issuing AgencyDevice ID
GS110841736123529 [Primary]

FDA Product Code

FQOTable, Operating-Room, Ac-Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-05-03
Device Publish Date2023-04-25

On-Brand Devices [Skytron LLC]

1084173612352960" Protective frame only, requires 4VB/4CM, Freedom, aluminum construction
10841736124298Active Assist Hold/Manual Control Assy Mounted on 3" LD VST, Freedom

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