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FDA 510(k) Applications Submitted by LASER CENTER DEV. CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K981235
04/03/1998
OCULOSTAT
LASER CENTER DEV. CORP.
K981063
03/23/1998
AUTOMATED CORNEAL TREPHINE
LASER CENTER DEV. CORP.
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