Sonogage Inc
FDA Regulatory Profile
Sonogage Inc appears in FDA public data with 1 recall, 1 510(k) clearance, 5 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2202-2013, Class II) was initiated on August 9, 2013. Its most recent 510(k) clearance was granted on January 30, 1986.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 1
- Inspections
- 5
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-2202-2013 | Class II | Sonogage EyeScan, A-Scan Biometer, Product Usage: A-Scan Biometer diagnostic device for measure | August 9, 2013 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K852862 | CORNEO-GAGE TWO | January 30, 1986 |