FISCHER MEDICAL

FDA Device Registration & Listing · Wheat Ridge, CO, US · Registration 3006188092

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
3006188092
FEI Number
3006188092
Entity Name
FISCHER MEDICAL
City/State/Country
Wheat Ridge, CO, US
Establishment Address
3990 Youngfield Street, Wheat Ridge, CO 80033, US
Establishment Type(s)
Remanufacture Medical Device,Manufacture Medical Device
Owner / Operator
FISCHER MEDICAL (Owner Number: 9099682)
Owner / Operator Contact Address
3990 Youngfield street, Wheat Ridge, CO 80033, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K991293
PMA Number
N/A

All Registered Proprietary Names

Hotchkiss LATOR EPSTIM SOFTWARE BLOOM DTU ELECTROPHYS. PROG. STIMU

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ERA Otoscope Ear, Nose, Throat Class 1 874.4770 2018-04-05
JOQ Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only) Cardiovascular Class 2 870.1750 2007-03-28

Official Correspondent

Wes Rogers

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

FISCHER MEDICAL
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
K932506 Rudolf Riester GmbH & Co. KG RI-SCOPE (S) 1993-10-08

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006188092. Last updated year: 2026. Please use registration number 3006188092 when referencing this establishment in official correspondence.
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