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ANGLED DELIVERY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K920589
510(k) Type
Traditional
Applicant
LASERSCOPE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1992
Days to Decision
79 days
Submission Type
Summary

ANGLED DELIVERY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K920589
510(k) Type
Traditional
Applicant
LASERSCOPE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1992
Days to Decision
79 days
Submission Type
Summary