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FDA 510(k) Applications Submitted by RYDER INTL. CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K962151
06/04/1996
RYDER LACRIMAL INTUBATIONSET
RYDER INTL. CORP.
K962611
07/03/1996
BARD EAGLE INFLATION DEVICE
RYDER INTL. CORP.
K953522
07/27/1995
USCI IDEAL PTCA KIT
RYDER INTL. CORP.
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