FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

3M 6830 ELECTRODE

K Number: K905539 · Decision May 28, 1991
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
436
Applicant Total
21
Review Days
168

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
3M 6830 ELECTRODE
K Number
K905539
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1320
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
3M Healthcare
Date Received
December 11, 1990
Decision Date
May 28, 1991
Product Code
GXY
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GXY Electrode, Cutaneous

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GXY), ordered by most recent decision date.

View all

Other Clearances by 3M Healthcare

K Number Device Name
K193110 3M Attest Vaporized Hydrogen Peroxide Tri-Metric Chemical Indicator 1348/1348E
K191355 3M™ High Fluid-Resistant Surgical Mask and 3M™ High Fluid-Resistant Procedure Mask
K180874 3M High Performance Surgical Mask, 3M High Performance Surgical Mask with Face Shield
K180404 3M Clarity Ultra Self-Ligating Brackets and Adhesive Coated Appliance System
K171116 3M™ VFlex™ Health Care Particulate Respirator and Surgical Mask , Models 1804/1804S
K153571 Cavilon Advanced High Endurance Skin Protectant
K140330 3M STERI-DRAPE FABRIC SURGICAL DRAPES
K140250 3M STERI-DRAPE CHG ANTIMICROBIAL INCISE DRAPE
K974445 3M RED DOT RESTING EKG ELECTRODE, CATALOG 2360
K980732 3M CDI QUICK-CELLS WITH HEPARIN TREATMENT
Search all 21 clearances from 3M Healthcare →