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ANGIOTOPO CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861241
510(k) Type
Traditional
Applicant
HOUSTON BIOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/1987
Days to Decision
279 days

ANGIOTOPO CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861241
510(k) Type
Traditional
Applicant
HOUSTON BIOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/1987
Days to Decision
279 days