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ULTRA CATHETER SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001115
510(k) Type
Traditional
Applicant
LYCO ENTERPRISES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/2000
Days to Decision
41 days
Submission Type
Statement

ULTRA CATHETER SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001115
510(k) Type
Traditional
Applicant
LYCO ENTERPRISES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/2000
Days to Decision
41 days
Submission Type
Statement