Last synced on 19 July 2024 at 11:05 pm

ALL SILICONE HEMATURIA CATHETER, MODELS 4861, 4862, 4863, 4864, 4865

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021142
510(k) Type
Traditional
Applicant
FORTUNE MEDICAL INSTRUMENT CORP.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
10/1/2002
Days to Decision
175 days
Submission Type
Statement

ALL SILICONE HEMATURIA CATHETER, MODELS 4861, 4862, 4863, 4864, 4865

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021142
510(k) Type
Traditional
Applicant
FORTUNE MEDICAL INSTRUMENT CORP.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
10/1/2002
Days to Decision
175 days
Submission Type
Statement