HMSClass I
Drum, Eye Knife Test
Ophthalmic · 21 CFR 886.4230
MDR events0All time
Recalls0All time
Registered firms1Currently listed
510(k) clearances1All time
Recent MDR events
0 adverse event reports on file
No MDR events on file for this product code.
Event type breakdown
No data available.
Most-reported manufacturers
No data available.
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
1 firms currently registered for this product code
510(k) clearances
1 clearances for this product code