Ryder Intl. Corp.
Ryder Intl. Corp. appears in FDA public data with 0 recalls, 10 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 21, 1996.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K962611 | BARD EAGLE INFLATION DEVICE | October 21, 1996 |
| K962151 | RYDER LACRIMAL INTUBATIONSET | September 18, 1996 |
| K953522 | USCI IDEAL PTCA KIT | April 17, 1996 |
| K920064 | OPTI-LENS CONTACT LENS CASE | March 4, 1992 |
| K915082 | OPTI-LENS(TM) CONTACT LENS CASE | January 13, 1992 |
| K881981 | ASSIST(TM) ASEPTIC SYRINGE IRRIGATION SYSTEM | August 2, 1988 |
| K870278 | CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695 | February 20, 1987 |
| K853727 | KESTREL CONTACT LENS STORAGE CASE(POLYSULFONE) | February 7, 1986 |
| K853729 | KESTREL CONTACT LENS STORAGE CASE(POLYSTYRENE) | December 13, 1985 |
| K853728 | KESTREL CONTACT LENS STORAGE CASE(NORYL) | December 13, 1985 |