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OTOSCOPE AND OPHTHALMOSCOPE DIAGNOSTIC INSTRUMENT KITS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093495
510(k) Type
Traditional
Applicant
AMERICAN DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2010
Days to Decision
374 days
Submission Type
Statement

OTOSCOPE AND OPHTHALMOSCOPE DIAGNOSTIC INSTRUMENT KITS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093495
510(k) Type
Traditional
Applicant
AMERICAN DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2010
Days to Decision
374 days
Submission Type
Statement