Last synced on 23 September 2022 at 11:05 pm

ALCON INDIRECT OPHTHALMOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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