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SHARPLAN-CONTEC EC-1000 ENDOSCOPY VIDEO CAMERA SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942740
510(k) Type
Traditional
Applicant
SHARPLAN LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/1994
Days to Decision
74 days
Submission Type
Summary