QUICK TUBE MEDICAL, LLC

FDA Device Registration & Listing · Knoxville, TN, US · Registration 3018114242

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3018114242
FEI Number
3018114242
Entity Name
QUICK TUBE MEDICAL, LLC
City/State/Country
Knoxville, TN, US
Establishment Address
3049 Kingston Pike, Knoxville, TN 37919, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Autterson (Owner Number: 10080886)
Owner / Operator Contact Address
3049 Kingston Pike, Knoxville, TN 37919, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GBX Catheter, Irrigation General, Plastic Surgery Class 1 878.4200 2023-05-16

Official Correspondent

Matthew Autterson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Autterson
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3018114242. Last updated year: 2026. Please use registration number 3018114242 when referencing this establishment in official correspondence.
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