Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1000151187

FEI Number

1000151187

Entity Name

AMERICAN CATHETER CORP

City/State/Country

Jupiter, FL, US

Establishment Address

357 Cypress Dr Ste 9, Jupiter, FL 33469, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

AMERICAN CATHETER CORP (Owner Number: 9083264)

Owner / Operator Contact Address

357 Cypress Dr, SUITE 9, Jupiter, FL 33458, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

American Catheter

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GBZ	Catheter, Cholangiography	General, Plastic Surgery	Class 1	878.4200	2006-02-22

Official Correspondent

todd CANTINE

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AMERICAN CATHETER CORP

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 1000151187. Last updated year: 2026. Please use registration number 1000151187 when referencing this establishment in official correspondence.