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FLEXIBLE PROCTOSIGMOIDOSCOPE, #FPS-3

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820790
510(k) Type
Traditional
Applicant
AMERICAN OPTICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1982
Days to Decision
9 days

FLEXIBLE PROCTOSIGMOIDOSCOPE, #FPS-3

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820790
510(k) Type
Traditional
Applicant
AMERICAN OPTICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1982
Days to Decision
9 days