510(k) K001869
K001869 is an FDA 510(k) premarket notification submitted by Medicotest A/S for the device "DIAGNOSTIC ELECTROMYOGRAPHY NEEDLE ELECTRODE, DISPOSABLE HYPODERMIC NEEDLE". The FDA issued a decision of Substantially Equivalent on September 18, 2000. The device falls under product code IKT (Electrode, Needle, Diagnostic Electromyograph), a Class II device regulated under 21 CFR 890.1385. Medicotest A/S has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 18, 2000
- Date Received
- June 20, 2000
- 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