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PEREGRINE OPTIPORT VITRECTOMY PROBE MODEL PD500.20

Page Type
Cleared 510(K)
510(k) Number
K980399
510(k) Type
Traditional
Applicant
PEREGRINE SURGICAL LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/1998
Days to Decision
87 days
Submission Type
Summary

PEREGRINE OPTIPORT VITRECTOMY PROBE MODEL PD500.20

Page Type
Cleared 510(K)
510(k) Number
K980399
510(k) Type
Traditional
Applicant
PEREGRINE SURGICAL LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/1998
Days to Decision
87 days
Submission Type
Summary