ClearanceBrief
Company ยท US

Ryder Intl. Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1985 to 1996. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
LRXCase, Contact Lens3
HPXLens, Contact (Polymethylmethacrylate)2
KODCatheter, Urological1
KOEDilator, Urethral1
LPNAccessories, Soft Lens Products1
MAVSyringe, Balloon Inflation1
OKSLacrimal Stents And Intubation Sets1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 21, 1996K962611BARD EAGLE INFLATION DEVICE
Ryder Intl. Corp.
KOE
Sep 18, 1996K962151RYDER LACRIMAL INTUBATIONSET
Ryder Intl. Corp.
OKS
Apr 17, 1996K953522USCI IDEAL PTCA KIT
Ryder Intl. Corp.
MAV
Mar 4, 1992K920064OPTI-LENS CONTACT LENS CASE
Ryder Intl. Corp.
LRX
Jan 13, 1992K915082OPTI-LENS(TM) CONTACT LENS CASE
Ryder Intl. Corp.
LRX
Aug 2, 1988K881981ASSIST(TM) ASEPTIC SYRINGE IRRIGATION SYSTEM
Ryder Intl. Corp.
KOD
Feb 20, 1987K870278CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695
Ryder Intl. Corp.
LPN
Feb 7, 1986K853727KESTREL CONTACT LENS STORAGE CASE(POLYSULFONE)
Ryder Intl. Corp.
LRX
Dec 13, 1985K853729KESTREL CONTACT LENS STORAGE CASE(POLYSTYRENE)
Ryder Intl. Corp.
HPX
Dec 13, 1985K853728KESTREL CONTACT LENS STORAGE CASE(NORYL)
Ryder Intl. Corp.
HPX

Latest recalls

DateFirm and productCodeLinked 510(k)
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