Last synced on 14 November 2025 at 11:06 pm

ECG MODULATOR

Page Type
Cleared 510(K)
510(k) Number
K922412
510(k) Type
Traditional
Applicant
MAGUIRE ENT., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/1992
Days to Decision
46 days
Submission Type
Statement

ECG MODULATOR

Page Type
Cleared 510(K)
510(k) Number
K922412
510(k) Type
Traditional
Applicant
MAGUIRE ENT., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/1992
Days to Decision
46 days
Submission Type
Statement