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VKG 2000 VIDEO KERATOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K893968
510(k) Type
Traditional
Applicant
TECHNITEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/1989
Days to Decision
101 days

VKG 2000 VIDEO KERATOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K893968
510(k) Type
Traditional
Applicant
TECHNITEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/1989
Days to Decision
101 days