Last synced on 30 May 2025 at 11:05 pm

HEMO-FLOW DOUBLE LUMEN CATHETER, MODELS HFS-24, HFS-28, HFS-32, HFS-36, HFS-40

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K994105
510(k) Type
Traditional
Applicant
MEDICAL COMPONENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2001
Days to Decision
667 days
Submission Type
Summary

HEMO-FLOW DOUBLE LUMEN CATHETER, MODELS HFS-24, HFS-28, HFS-32, HFS-36, HFS-40

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K994105
510(k) Type
Traditional
Applicant
MEDICAL COMPONENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2001
Days to Decision
667 days
Submission Type
Summary