Last synced on 18 April 2025 at 11:05 pm

.25' ULTRA-SELECT GUIDEWIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922060
510(k) Type
Traditional
Applicant
MICROVENA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1993
Days to Decision
295 days
Submission Type
Statement

.25' ULTRA-SELECT GUIDEWIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922060
510(k) Type
Traditional
Applicant
MICROVENA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1993
Days to Decision
295 days
Submission Type
Statement