Fischer Medical Supply

FDA Device Registration & Listing · Moorpark, CA, US · Registration 3022698313

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
3022698313
FEI Number
3022698313
Entity Name
Fischer Medical Supply
City/State/Country
Moorpark, CA, US
Establishment Address
5400 Atlantis Court, Suite C, Moorpark, CA 93021, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Fischer Medical Supply (Owner Number: 10085209)
Owner / Operator Contact Address
5400 Atlantis Court, Suite C, Moorpark, CA 93021, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K191436
PMA Number
N/A

All Registered Proprietary Names

The Fischer

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EGJ Device, Iontophoresis, Other Uses Physical Medicine Class 2 890.5525 2023-01-04

Official Correspondent

Jennifer Jacobellis

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K842483 Santa Barbara Medco, Inc. SANTA BARBARA MEDCO-LANTOPHORETIC APPLIC 1984-08-31

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022698313. Last updated year: 2026. Please use registration number 3022698313 when referencing this establishment in official correspondence.
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