TECA MYOJECT DISPOSABLE NEEDLE ELECTRODES— 510(k) K973444
Substantially EquivalentMedelec, Inc. D.B.A. Teca Corp.
FDA 510(k) clearance K973444 for TECA MYOJECT DISPOSABLE NEEDLE ELECTRODES, Substantially Equivalent on 1997-11-20. Applicant: Medelec, Inc. D.B.A. Teca Corp..
Clearance details
- Applicant
- Medelec, Inc. D.B.A. Teca Corp.
- Product code
- Code IKT
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Pleasantville, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.