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Surgistar, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
5
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K030891
SURGISTAR MICROKERATOME BLADE, MODEL NO. 2400-LSK
June 17, 2003
K992978
RICROKERATOME BLADE
November 16, 1999
K941747
SURGISTAR TROCARS
July 1, 1994
K923689
SURGISTAR BLADES
September 9, 1992