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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