VOLTAS MEDICAL LLC

FDA Device Registration & Listing · Cottage Grove, MN, US · Registration 3043198445

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
3043198445
FEI Number
3043198445
Entity Name
VOLTAS MEDICAL LLC
City/State/Country
Cottage Grove, MN, US
Establishment Address
8200 97th St S, Cottage Grove, MN 55016, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Voltas Medical LLC (Owner Number: 10095699)
Owner / Operator Contact Address
8200 97th Street, Cottage Grove, MN 55016, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

FloPatch

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DPW Flowmeter, Blood, Cardiovascular Cardiovascular Class 2 870.2100 2026-04-15

Official Correspondent

Bhaskar Siyyadri

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Voltas Medical LLC
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
K903633 Transonic Systems, Inc. ADVANCE LASER FLOWMETER, ALF 21 1990-10-09
K182494 Laser Associated Sciences, Inc. FlowMet-R 2019-02-27

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043198445. Last updated year: 2026. Please use registration number 3043198445 when referencing this establishment in official correspondence.
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