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PRIZM KERATOME BLADE, MODEL MK8512M2

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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