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CLINICAL WIDEFIELD SPECULAR MICRISCOPE 500

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852150
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/1985
Days to Decision
17 days

CLINICAL WIDEFIELD SPECULAR MICRISCOPE 500

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852150
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/1985
Days to Decision
17 days