Last synced on 25 January 2026 at 3:41 am

FB-18X, FIBER BRONCHOSCOPE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951199
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1995
Days to Decision
25 days
Submission Type
Summary

FB-18X, FIBER BRONCHOSCOPE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951199
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1995
Days to Decision
25 days
Submission Type
Summary