EAR SPECULI— 510(k) K822164
Substantially EquivalentKelleher Corp.
FDA 510(k) clearance K822164 for EAR SPECULI, Substantially Equivalent on 1982-08-11. Applicant: Kelleher Corp.. Device class: 1.
Clearance details
- Applicant
- Kelleher Corp.
- Product code
- Code EPY
- Device class
- Class 1
- Regulation
- 21 CFR 878.1800
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
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