ELECTROMED, INC.

FDA Device Registration & Listing · NEW PRAGUE, MN, US · Registration 2134852

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
2134852
FEI Number
3003007907
Entity Name
ELECTROMED, INC.
City/State/Country
NEW PRAGUE, MN, US
Establishment Address
502 SIXTH AVE. N.W., NEW PRAGUE, MN 56071, US
Establishment Type(s)
Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
ELECTROMED, INC. (Owner Number: 9034783)
Owner / Operator Contact Address
502 SIXTH AVE., NW, --, New Prague, MN 56071, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K222496
PMA Number
N/A

All Registered Proprietary Names

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Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BYI Percussor, Powered-Electric Anesthesiology Class 2 868.5665 1999-10-15
BYI Percussor, Powered-Electric Anesthesiology Class 2 868.5665 2014-12-15
BYI Percussor, Powered-Electric Anesthesiology Class 2 868.5665 2023-01-04

Official Correspondent

Amy Yanta

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ELECTROMED, INC.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2134852. Last updated year: 2026. Please use registration number 2134852 when referencing this establishment in official correspondence.
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