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ALCON INDIRECT OPHTHALMOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K822104
510(k) Type
Traditional
Applicant
ALCON LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1982
Days to Decision
22 days

ALCON INDIRECT OPHTHALMOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K822104
510(k) Type
Traditional
Applicant
ALCON LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1982
Days to Decision
22 days