Last synced on 6 June 2025 at 11:06 pm

SMARTSCAN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K941841
510(k) Type
Traditional
Applicant
LASERSCOPE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/1994
Days to Decision
124 days
Submission Type
Summary

SMARTSCAN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K941841
510(k) Type
Traditional
Applicant
LASERSCOPE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/1994
Days to Decision
124 days
Submission Type
Summary