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INNOVATECH STRAIGHT LASER PROBE, MODEL 420-10

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032703
510(k) Type
Traditional
Applicant
Innovatech Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2003
Days to Decision
52 days
Submission Type
Summary

INNOVATECH STRAIGHT LASER PROBE, MODEL 420-10

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032703
510(k) Type
Traditional
Applicant
Innovatech Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2003
Days to Decision
52 days
Submission Type
Summary