Vision Quest Industries, Inc.
Vision Quest Industries, 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 March 23, 2015.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K142236 | BioniCare Hand System | March 23, 2015 |
| K090532 | T.E.A.R. TECH3 | November 13, 2009 |
| K072799 | TARGET STERILE ELECTRODE | April 24, 2008 |
| K041092 | FAST START TENS, MODEL FS 3001 | July 1, 2004 |
| K030507 | T.E.A.R. TECH3 MODEL #44TT03 | May 20, 2003 |
| K982388 | SURGI STIM | September 14, 1998 |