Last synced on 16 August 2024 at 11:05 pm

PENTAX PNE- ULTRA-SLIM UPPER G.I. FIBERSCOPE FG-23

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K850020
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/1985
Days to Decision
186 days

PENTAX PNE- ULTRA-SLIM UPPER G.I. FIBERSCOPE FG-23

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K850020
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/1985
Days to Decision
186 days