Last synced on 4 February 2023 at 10:33 pm

ENDOSCOPIC INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K791052
510(k) Type
Traditional
Applicant
EDER INSTRUMENT CO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1979
Days to Decision
58 days

ENDOSCOPIC INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K791052
510(k) Type
Traditional
Applicant
EDER INSTRUMENT CO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1979
Days to Decision
58 days