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MICROPLEX COIL SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K012145
510(k) Type
Traditional
Applicant
MICROVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/29/2001
Days to Decision
111 days
Submission Type
Summary

MICROPLEX COIL SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K012145
510(k) Type
Traditional
Applicant
MICROVENTION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/29/2001
Days to Decision
111 days
Submission Type
Summary