Last synced on 9 May 2025 at 11:05 pm

AZUR PURE PERIPHERAL COIL SYSTEM, PUSHABLE 18 AZUR PURE PERIPHERAL COIL SYSTEM, PUSHABLE 35

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122543
510(k) Type
Traditional
Applicant
MICROVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/2012
Days to Decision
99 days
Submission Type
Summary

AZUR PURE PERIPHERAL COIL SYSTEM, PUSHABLE 18 AZUR PURE PERIPHERAL COIL SYSTEM, PUSHABLE 35

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122543
510(k) Type
Traditional
Applicant
MICROVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/2012
Days to Decision
99 days
Submission Type
Summary