Biovision, Inc.
Biovision, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 16, 2004.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K042083 | MODIFICATION TO VISITOME 20-10 MICROKERATOME | November 16, 2004 |
| K014000 | VISTITOME 20-10 MICROKERATOME | March 11, 2002 |
| K974392 | LEADFIX BIORESORBABLE MEMBRANCE PIN SYSTEM | January 30, 1998 |
| K926251 | B-SCAN OPTHALMIC ULTRASOUND IMAGING SYSTEM | September 14, 1993 |
| K910027 | CRYSTAL FOCUS EMERALD LASER SLT MCX 1.5 CONVEX PRO | September 25, 1991 |
| K901636 | DIAMOND ND:YAG OPHTHALMIC LASER | June 22, 1990 |