Last synced on 27 January 2023 at 11:04 pm

LT-300 SD Digital Video Colposcope

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170446
510(k) Type
Traditional
Applicant
Lutech Industries, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2017
Days to Decision
96 days
Submission Type
Statement

LT-300 SD Digital Video Colposcope

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170446
510(k) Type
Traditional
Applicant
Lutech Industries, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2017
Days to Decision
96 days
Submission Type
Statement