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TWO CHANNEL GASTROFIBERSCOPE FG-36T

Page Type
Cleared 510(K)
510(k) Number
K833924
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/1984
Days to Decision
82 days

TWO CHANNEL GASTROFIBERSCOPE FG-36T

Page Type
Cleared 510(K)
510(k) Number
K833924
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/1984
Days to Decision
82 days