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MICRO-GUIDE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884337
510(k) Type
Traditional
Applicant
CATHETER RESEARCH C/O BURDITT, BOWLES & RADZIUS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/5/1989
Days to Decision
83 days

MICRO-GUIDE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884337
510(k) Type
Traditional
Applicant
CATHETER RESEARCH C/O BURDITT, BOWLES & RADZIUS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/5/1989
Days to Decision
83 days