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PARASCAN SCANNING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K964520
510(k) Type
Traditional
Applicant
LASERSCOPE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1997
Days to Decision
90 days
Submission Type
Summary

PARASCAN SCANNING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K964520
510(k) Type
Traditional
Applicant
LASERSCOPE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1997
Days to Decision
90 days
Submission Type
Summary