510(k) K163343
K163343 is an FDA 510(k) premarket notification submitted by Icare Finland OY for the device "Icare HOME tonometer". The FDA issued a decision of Substantially Equivalent on March 21, 2017. The device falls under product code HKY (Tonometer, Manual), a Class II device regulated under 21 CFR 886.1930. Icare Finland OY has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 21, 2017
- Date Received
- November 29, 2016
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tonometer, Manual
- Device Class
- Class II
- Regulation Number
- 886.1930
- Review Panel
- OP
- Submission Type