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FDA 510(k) Applications Submitted by SULZER OSCOR, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990142
01/19/1999
HT, MODEL HT PB
SULZER OSCOR, INC.
K970497
02/10/1997
PACE 101H
SULZER OSCOR, INC.
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