Opticon Medical, Inc.
Opticon Medical, Inc. appears in FDA public data with 0 recalls, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 17, 2004.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K041983 | OPTION-VM URINARY CATHETER/ADPATER, MODELS MV39016, MVA39016 | November 17, 2004 |
| K033830 | OPTION-VF URINARY CATHETER WITH ADAPTOR, MODEL FVA14218; OPTION-V CONTINUOUS DRAINAGE ADAPTOR, MODEL | January 9, 2004 |
| K023090 | OPTION-VF URINARY CATHETER, FV14218 | March 19, 2003 |
| K970716 | OPTICON DIRECT MALE URINARY CATHETER FOR CONTINUOUS DRAINAGE | May 16, 1997 |
| K930194 | HEMOSTASIS VALVE AND TUBING SET | September 22, 1993 |
| K904999 | WEINGARTEN TM CAPNOGRAPHIC INTUBATION STYLETTE | January 26, 1993 |
| K895955 | LOPER CELIAC PLEXUS BLOCK CATHETER KIT | February 22, 1990 |
| K895476 | OPTION EPIDURAL CATHETERS | January 19, 1990 |