Last synced on 14 November 2025 at 11:06 pm

UROTOPO CATHETER

Page Type
Cleared 510(K)
510(k) Number
K861200
510(k) Type
Traditional
Applicant
HOUSTON BIOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/1986
Days to Decision
23 days

UROTOPO CATHETER

Page Type
Cleared 510(K)
510(k) Number
K861200
510(k) Type
Traditional
Applicant
HOUSTON BIOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/1986
Days to Decision
23 days