Last synced on 14 November 2025 at 11:06 pm

PENTAX FG-34JA GASTROFIBERSCOPE

Page Type
Cleared 510(K)
510(k) Number
K832007
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/1983
Days to Decision
49 days

PENTAX FG-34JA GASTROFIBERSCOPE

Page Type
Cleared 510(K)
510(k) Number
K832007
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/1983
Days to Decision
49 days