Last synced on 2 December 2022 at 11:04 pm

FIEGERT ENDOTECH CYSTOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970892
510(k) Type
Traditional
Applicant
FIEGERT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/1997
Days to Decision
55 days
Submission Type
Statement

FIEGERT ENDOTECH CYSTOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970892
510(k) Type
Traditional
Applicant
FIEGERT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/1997
Days to Decision
55 days
Submission Type
Statement