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PENTAX FD-34A DUODENOFIBERSCOPE

Page Type
Cleared 510(K)
510(k) Number
K832006
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1983
Days to Decision
39 days

PENTAX FD-34A DUODENOFIBERSCOPE

Page Type
Cleared 510(K)
510(k) Number
K832006
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1983
Days to Decision
39 days