SELECTIVE MED COMPONENTS, INC. BUFFERED IONTOPHORESIS DRUG DELIVERY SYSTEM ELECTRODES - I7
by Selectivemed Components, Inc.
510(k) K031053
Active
Valid until
No expiry
FDA recalls
None ongoingDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK031053 | Date20 May 2003 | StatusActive |
Recalls
-
- Terminated Z-0799-05
The conductor portion of the electrode is installed backwards, with the plastic and silver portions of the electrode reversed.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- EGJ
- Device Class
- Class II
- Regulation
- 21 CFR Part 890.5525
- Advisory Committee
- Physical Medicine
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 25 Sep 2026
The Buffered Iontophoresis Drug Delivery System Electrodes are devices designed to introduce soluble salts and other drugs into the body as an alternative to hypodermic injection. The system consists of an active drug delivery electrode and a passive return electrode, facilitating the local administration of ionic drug solutions into the body for medical purposes.
These electrodes are designed for single-patient, one-time use and are available in multiple sizes and shapes. The device is classified under product code EGJ for Device, Iontophoresis, Other Uses and received FDA 510(k) clearance with K-number K031053 on May 20, 2003.
Other devices from Selectivemed Components, Inc.
Questions
AI-generated answers, 25 Sep 2026
What are Buffered Iontophoresis Drug Delivery System Electrodes used for?
These electrodes are designed to introduce soluble salts and other drugs into the body as an alternative to hypodermic injection, facilitating local administration of ionic drug solutions for medical purposes.
Are these electrodes reusable or single-use?
The Buffered Iontophoresis Drug Delivery System Electrodes are designed for single-patient, one-time use only and should not be reused between different patients.
What sizes and models are available for these electrodes?
The electrodes are available in multiple sizes and shapes, specifically in Models I20, I30, I40, I50, and I7, to accommodate various treatment needs and anatomical considerations.
What is the regulatory status of these electrodes?
The device is classified under product code EGJ for Device, Iontophoresis, Other Uses and received FDA 510(k) clearance with K-number K031053 on May 20, 2003.