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REUSABLE VITRECTOMY PROBE

Page Type
Cleared 510(K)
510(k) Number
K970670
510(k) Type
Traditional
Applicant
ALTEX VISION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/1997
Days to Decision
71 days
Submission Type
Statement

REUSABLE VITRECTOMY PROBE

Page Type
Cleared 510(K)
510(k) Number
K970670
510(k) Type
Traditional
Applicant
ALTEX VISION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/1997
Days to Decision
71 days
Submission Type
Statement