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PRIZM KERATOME BLADE, MODEL MK8512M2

Page Type
Cleared 510(K)
510(k) Number
K033236
510(k) Type
Traditional
Applicant
SURGIN SURGICAL INSTRUMENTATION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/2004
Days to Decision
172 days
Submission Type
Statement

PRIZM KERATOME BLADE, MODEL MK8512M2

Page Type
Cleared 510(K)
510(k) Number
K033236
510(k) Type
Traditional
Applicant
SURGIN SURGICAL INSTRUMENTATION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/2004
Days to Decision
172 days
Submission Type
Statement