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FDA 510(k) Applications Submitted by ALAIN DUPRAT
FDA 510(k) Number
Submission Date
Device Name
Applicant
K960395
01/29/1996
PLANCON MIRCOLAMELLAR KERATOME
PLANCON INSTRUMENTS
K970377
02/03/1997
PLANCON MICROLAMELLAR KERATOME (SINGLE PIECE KERATOME HEAD WITH ACCESSORIES)
PLANCON INSTRUMENTS
K980924
03/11/1998
PLANCON MICROLAMELLAR KERATOME EVOLUTION
PLANCON INSTRUMENTS
K981741
05/18/1998
CARRIAZO BARRAQUER MICROKERATOME
MORIA, INC.
K981742
05/18/1998
ONE UP DISPOSABLE KERATOME HEAD
MORIA, INC.
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