Endooptiks, Inc.
Endooptiks, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 3, 2009.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K083788 | ENDO OPTIKS UROLOGICAL CATHETER FOR ENDOSCOPY, MODEL SESSR | March 3, 2009 |
| K042918 | MICROPROBE LASER AND ENDOSCOPY SYSTEM, MODEL E2 | November 22, 2004 |
| K003151 | MICROPOBE SERIES OF LASERS AND ACCESSORIES | January 8, 2001 |
| K945081 | TRANSTYMPANIC ENDOSCOPE | March 6, 1995 |
| K922917 | ENDOPROBES | September 28, 1992 |