Spare MS 700 Tens Electrode
by Lectec Corp.
510(k) K881871
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK881871 | Date16 Jun 1988 | StatusActive |
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- GXY
- Device Class
- Class II
- Regulation
- 21 CFR Part 882.1320
- Advisory Committee
- Neurology
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 24 Sep 2026
The Spare MS 700 Tens Electrode is a medical device designed for use in transcutaneous electrical nerve stimulation therapy. It functions as an interface to deliver electrical impulses to the patient's skin for therapeutic purposes.
This device is identified under FDA 510(k) clearance number K881871. It is manufactured by Lectec Corp. and is classified under the neurology advisory committee.
Other devices from Lectec Corp.
Questions
AI-generated answers, 24 Sep 2026
What is the primary function of the Spare MS 700 TENS Electrode?
This device serves as an interface for transcutaneous electrical nerve stimulation therapy. It is designed to deliver electrical impulses directly to the patient's skin to facilitate therapeutic treatment.
Who is the manufacturer of this TENS electrode?
The Spare MS 700 TENS Electrode is manufactured by Lectec Corp., located in Minnetonka, Minnesota.
What is the regulatory status of the Spare MS 700 TENS Electrode?
This device is identified under FDA 510(k) clearance number K881871. It was reviewed under the neurology advisory committee and determined to be substantially equivalent to existing devices.