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I SIGHT 2020 ENDOSCOPIC & SURGICAL VIDEO CAMERA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934097
510(k) Type
Traditional
Applicant
SHARPLAN LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/1994
Days to Decision
168 days
Submission Type
Summary