RS MEDICAL

FDA Device Registration & Listing · VANCOUVER, WA, US · Registration 1644243

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
1644243
FEI Number
1000117825
Entity Name
RS MEDICAL
City/State/Country
VANCOUVER, WA, US
Establishment Address
14101 Se 1st St, VANCOUVER, WA 98684, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
RS MEDICAL (Owner Number: 9001699)
Owner / Operator Contact Address
14001 S.E. FIRST ST., --, Vancouver, WA 98684, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K112348
PMA Number
N/A

All Registered Proprietary Names

Pronex Cervical Traction Device RS-4i Plus Sequential Stimulator RS-4s Stimulator

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HST Apparatus, Traction, Non-Powered Orthopedic Class 1 888.5850 2008-10-24
IPF Stimulator, Muscle, Powered Physical Medicine Class 2 890.5850 2012-06-19
LIH Interferential Current Therapy Neurology Class 2 882.5890 2012-06-19

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

RS 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
K030403 Cefar Medical AB CEFAR REHAB 2 AND REHAB 2 PRO 2003-07-17
K231440 Shenzhen Roundwhale Technology Co. , Ltd. Combo Electrotherapy Device 2023-11-03
K820884 Nitron Electronics ELECTRICAL MUSCLE STIMULATOR 1982-04-29
K201958 Therasigma, LLC ETD Family of Electrotherapy Devices 2020-08-04
K964028 Mettler Electronics Corp. SYS STIM 226 1997-02-03

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1644243. Last updated year: 2026. Please use registration number 1644243 when referencing this establishment in official correspondence.
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