Last synced on 19 July 2024 at 11:05 pm

BRONCHOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954707
510(k) Type
Traditional
Applicant
FUJINON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1995
Days to Decision
41 days
Submission Type
Statement

BRONCHOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954707
510(k) Type
Traditional
Applicant
FUJINON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1995
Days to Decision
41 days
Submission Type
Statement