510(k) K912283

DETACHABLE, DISPOSABLE MONOPOLAR NEEDLE ELECTRODE by Chalgren Enterprises, Inc. — Product Code IKT

K912283 is an FDA 510(k) premarket notification submitted by Chalgren Enterprises, Inc. for the device "DETACHABLE, DISPOSABLE MONOPOLAR NEEDLE ELECTRODE". The FDA issued a decision of Substantially Equivalent on March 16, 1992. The device falls under product code IKT (Electrode, Needle, Diagnostic Electromyograph), a Class II device regulated under 21 CFR 890.1385. Chalgren Enterprises, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 16, 1992
Date Received
May 23, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrode, Needle, Diagnostic Electromyograph
Device Class
Class II
Regulation Number
890.1385
Review Panel
NE
Submission Type