HAND KERATOSCOPE— 510(k) K821080
Substantially EquivalentMedical Equipment Designs, Inc.
FDA 510(k) clearance K821080 for HAND KERATOSCOPE, Substantially Equivalent on 1982-05-24. Applicant: Medical Equipment Designs, Inc.. Device class: 1.
Clearance details
- Applicant
- Medical Equipment Designs, Inc.
- Product code
- Code HLR
- Device class
- Class 1
- Regulation
- 21 CFR 886.1350
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code HLR
view allMore clearances from Medical Equipment Designs, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.