Ryder Intl. Corp.
Ryder Intl. Corp. holds FDA 510(k) medical device clearances, first cleared 1985, most recent 1996.
Top product codes for Ryder Intl. Corp.
Recent clearances by Ryder Intl. Corp.
- K962611 — BARD EAGLE INFLATION DEVICE
- K962151 — RYDER LACRIMAL INTUBATIONSET
- K953522 — USCI IDEAL PTCA KIT
- K920064 — OPTI-LENS CONTACT LENS CASE
- K915082 — OPTI-LENS(TM) CONTACT LENS CASE
- K881981 — ASSIST(TM) ASEPTIC SYRINGE IRRIGATION SYSTEM
- K870278 — CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695
- K853727 — KESTREL CONTACT LENS STORAGE CASE(POLYSULFONE)
- K853728 — KESTREL CONTACT LENS STORAGE CASE(NORYL)
- K853729 — KESTREL CONTACT LENS STORAGE CASE(POLYSTYRENE)
Data sourced from openFDA. This site is unofficial and independent of the FDA.