AUTOFOCUS PROBE FOR USE WITH ULTRASOUND AUTOSECTOR SYSTEM— 510(k) K837046
Substantially EquivalentTechnicare Corp.
FDA 510(k) clearance K837046 for AUTOFOCUS PROBE FOR USE WITH ULTRASOUND AUTOSECTOR SYSTEM, Substantially Equivalent on 1983-04-01. Applicant: Technicare Corp..
Clearance details
- Applicant
- Technicare Corp.
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Solon, OH, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.