Last synced on 25 November 2022 at 11:04 pm

PENTAX UPPER G.I. FIBERSCOPE, #FG-34

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K810007
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/1981
Days to Decision
10 days

PENTAX UPPER G.I. FIBERSCOPE, #FG-34

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K810007
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/1981
Days to Decision
10 days