EYE TRAY— 510(k) K912105
Substantially EquivalentMedical Device Inspection Co., Inc.
FDA 510(k) clearance K912105 for EYE TRAY, Substantially Equivalent on 1991-08-29. Applicant: Medical Device Inspection Co., Inc.. Device class: 1.
Clearance details
- Applicant
- Medical Device Inspection Co., Inc.
- Product code
- Code LRP
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Great Neck, NY, US
Recent devices under product code LRP
view allMore clearances from Medical Device Inspection Co., Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.