GLOTTAL FREQUENCY ANALYSER— 510(k) K841832
Substantially EquivalentTeltec Electronic Equipment AB
FDA 510(k) clearance K841832 for GLOTTAL FREQUENCY ANALYSER, Substantially Equivalent on 1984-07-18. Applicant: Teltec Electronic Equipment AB. Device class: 2.
Clearance details
- Applicant
- Teltec Electronic Equipment AB
- Product code
- Code KLX
- Device class
- Class 2
- Regulation
- 21 CFR 874.1325
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code KLX
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