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ALL SILICONE SUPRA-PUBIA CATHETER, MODELS 4880/4890

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K014002
510(k) Type
Traditional
Applicant
FORTUNE MEDICAL INSTRUMENT CORP.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
3/4/2002
Days to Decision
90 days
Submission Type
Statement

ALL SILICONE SUPRA-PUBIA CATHETER, MODELS 4880/4890

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K014002
510(k) Type
Traditional
Applicant
FORTUNE MEDICAL INSTRUMENT CORP.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
3/4/2002
Days to Decision
90 days
Submission Type
Statement