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LT-300 Video Colposcope

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143119
510(k) Type
Traditional
Applicant
Lutech Industries, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2014
Days to Decision
49 days
Submission Type
Statement

LT-300 Video Colposcope

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143119
510(k) Type
Traditional
Applicant
Lutech Industries, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2014
Days to Decision
49 days
Submission Type
Statement