Last synced on 6 June 2025 at 11:06 pm

INTRODUCER, PERCUTANEOUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K870907
510(k) Type
Traditional
Applicant
MEDFUSION SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/1987
Days to Decision
35 days

INTRODUCER, PERCUTANEOUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K870907
510(k) Type
Traditional
Applicant
MEDFUSION SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/1987
Days to Decision
35 days