ACOUSTIQ LISTENING DEVICE— 510(k) K904755
Substantially EquivalentKrueger Laboratories
FDA 510(k) clearance K904755 for ACOUSTIQ LISTENING DEVICE, Substantially Equivalent on 1991-01-29. Applicant: Krueger Laboratories.
Clearance details
- Applicant
- Krueger Laboratories
- Product code
- Code LZI
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tempe, AZ, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.