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FDA 510(k) Applications Submitted by TRANSIDYNE GENERAL CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K961217
03/28/1996
BODILY FLUID DISPOSAL KIT
TRANSIDYNE GENERAL CORP.
K955658
12/12/1995
LACERATION TRAY
TRANSIDYNE GENERAL CORP.
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