Last synced on 14 November 2025 at 11:06 pm

ALL SILICONE 2-WAY & 3-WAY FOLY BALLOON CATHETER AND NELATON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K980919
510(k) Type
Traditional
Applicant
FORTUNE MEDICAL INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1998
Days to Decision
20 days
Submission Type
Statement

ALL SILICONE 2-WAY & 3-WAY FOLY BALLOON CATHETER AND NELATON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K980919
510(k) Type
Traditional
Applicant
FORTUNE MEDICAL INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1998
Days to Decision
20 days
Submission Type
Statement